Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP919793.RAC0-F1MbNMpZDEpOtGpo5U8TgoW5c3tIrN7u9a4C1lvo130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919793.RAC0-F1MbNMpZDEpOtGpo5U8TgoW5c3tIrN7u9a4C1lvo130_provenance.
• NP633345.RAf8Uti7QDpoJQdBvk7NcoLWDXkES4U-EpP6MAtvrYua0130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP633345.RAf8Uti7QDpoJQdBvk7NcoLWDXkES4U-EpP6MAtvrYua0130_provenance.
• NP547132.RABfK4jBmPvGjPNvl9O3fbJWkX32pI0kxO1GND6ju31gA130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP547132.RABfK4jBmPvGjPNvl9O3fbJWkX32pI0kxO1GND6ju31gA130_provenance.
• NP593618.RAn5XpebotoQKcpDDCyHiBqT8hzm7gaLRwTRx4OM51iLQ130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP593618.RAn5XpebotoQKcpDDCyHiBqT8hzm7gaLRwTRx4OM51iLQ130_provenance.
• NP783816.RAsm4SJXXMSt-XoYpWi610G17MSE3IXs-KvqeB68AoyL4130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783816.RAsm4SJXXMSt-XoYpWi610G17MSE3IXs-KvqeB68AoyL4130_provenance.
• NP648529.RAbxj6_83UsTrX0typh5bkXPPDnq5tE-U2BB35d6wZqQU130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648529.RAbxj6_83UsTrX0typh5bkXPPDnq5tE-U2BB35d6wZqQU130_provenance.
• NP172588.RA7adzzgQhf0dJOBMKlyfl3_LlayCxfis_UTAxClXZgG4130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP172588.RA7adzzgQhf0dJOBMKlyfl3_LlayCxfis_UTAxClXZgG4130_provenance.
• NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP405162.RA8BGEzoQRjNa2BCTTJlcErCCokCxgDe2BfgKNlxT9kRk130_provenance.
• NP917223.RAnSRvnzYUf2tA7y-uUPOcr3ob19UjFrCU2T2hRKxcM4E130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP917223.RAnSRvnzYUf2tA7y-uUPOcr3ob19UjFrCU2T2hRKxcM4E130_provenance.
• assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239413.RAfzxQL3QPHQJfaXFNSFXoD83_Y816lHdUrXN2gjw11FA130_provenance.
• NP350748.RAbpB6vt9dNFLHL22XQORdUrJUCyYWQJnm20D_MEOZaBM130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP350748.RAbpB6vt9dNFLHL22XQORdUrJUCyYWQJnm20D_MEOZaBM130_provenance.
• NP606194.RAYCmQ0drlwRjCw39dih0gioV_Mx60H4ZPwLVoalrBak8130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP606194.RAYCmQ0drlwRjCw39dih0gioV_Mx60H4ZPwLVoalrBak8130_provenance.
• NP491342.RAG1B01Jeaa39xH7OgYNitI6trtGfZxTX2TPFrz8RbT2I130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP491342.RAG1B01Jeaa39xH7OgYNitI6trtGfZxTX2TPFrz8RbT2I130_provenance.
• assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284920.RAX5Lnq9AB8To2SYmvtPlOUhfqGQNO9fTYfM-ucTcrY6k130_provenance.
• NP284927.RAQJraa2e8l80BAobzb5nLRtdMubhgb8Fqr2mJaX4drrE130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284927.RAQJraa2e8l80BAobzb5nLRtdMubhgb8Fqr2mJaX4drrE130_provenance.
• assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP420723.RAmIPemMJIeio0uaAI4Cnn_vvc0FPPEEZoNOPGn5oH8IU130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420723.RAmIPemMJIeio0uaAI4Cnn_vvc0FPPEEZoNOPGn5oH8IU130_provenance.
• NP505755.RAmzUG78NMz4B2RcpwENW0kpvKQg_TGnQBGnGnlF1amHs130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP505755.RAmzUG78NMz4B2RcpwENW0kpvKQg_TGnQBGnGnlF1amHs130_provenance.
• NP284923.RApmollWulzLMejpZjXusMhU42dOPojVuP0v7HOV6Owh8130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284923.RApmollWulzLMejpZjXusMhU42dOPojVuP0v7HOV6Owh8130_provenance.
• NP284924.RApSdAtTheUMr9ml8qrP8UuzHT8aJtEJZFSA_qXaiqCyg130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284924.RApSdAtTheUMr9ml8qrP8UuzHT8aJtEJZFSA_qXaiqCyg130_provenance.
• NP284930.RAghwF-P5XNsDZUmh4rNnMopccM1VKPaEed1Tpzjb7bR0130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284930.RAghwF-P5XNsDZUmh4rNnMopccM1VKPaEed1Tpzjb7bR0130_provenance.
• NP397729.RA_ytVAm922EF8RT4yYbkdTR-czW9xmPLLpJWWhH_6yiM130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397729.RA_ytVAm922EF8RT4yYbkdTR-czW9xmPLLpJWWhH_6yiM130_provenance.
• NP566715.RA1XEzvG3PaBkxO8JEXbmzyLpH9ky1xQr6R1wUhMtVOxU130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP566715.RA1XEzvG3PaBkxO8JEXbmzyLpH9ky1xQr6R1wUhMtVOxU130_provenance.
• NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP301834.RAHGx_Xlc8HVaSPtNRGeRc4HdelolhvJZ6dODgyLAmu30130_provenance.
• NP808612.RAEdeXuX6OZLOUwKeZFiS8J5bCL3WNkU2tDgBAcGDuY-c130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808612.RAEdeXuX6OZLOUwKeZFiS8J5bCL3WNkU2tDgBAcGDuY-c130_provenance.
• NP964086.RAGxo1QJEbmnFUXqRVxiuK9RSCr46wk0ZN-Uk23Q1ZRtI130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP964086.RAGxo1QJEbmnFUXqRVxiuK9RSCr46wk0ZN-Uk23Q1ZRtI130_provenance.
• NP406974.RAEp5DJRIJLEegJ8eP9cYEWffDugHN3vRiwSIFEpe0zqE130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP406974.RAEp5DJRIJLEegJ8eP9cYEWffDugHN3vRiwSIFEpe0zqE130_provenance.
• NP949904.RAzOPTSr7I9rOtfILyC3bW1aEiugtF-VHsZc6PKe6Hg-M130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP949904.RAzOPTSr7I9rOtfILyC3bW1aEiugtF-VHsZc6PKe6Hg-M130_provenance.
• NP284925.RAEI-NePMS1pSgAaQ6SNgNglTItuV9co8rpVTNTwRe0FA130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284925.RAEI-NePMS1pSgAaQ6SNgNglTItuV9co8rpVTNTwRe0FA130_provenance.
• NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284926.RAOQ3hYRn9bwAtFflUfc33-9g9m8uDWHECHFkH9FO22fg130_provenance.
• NP284928.RANiCGwbgacjdZR2mxLVhHqzTSlDSaFCNTn5ZTgxMss2w130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284928.RANiCGwbgacjdZR2mxLVhHqzTSlDSaFCNTn5ZTgxMss2w130_provenance.
• NP284921.RA4s42MPgdU3IAKgYQ6BiwRxLqNUh97-SuKwSCWumNqg8130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284921.RA4s42MPgdU3IAKgYQ6BiwRxLqNUh97-SuKwSCWumNqg8130_provenance.
• NP284922.RA4WT9iX4l-YWyglRUB6UXo2qXa_hYIhiRPbMpT_YY8J4130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284922.RA4WT9iX4l-YWyglRUB6UXo2qXa_hYIhiRPbMpT_YY8J4130_provenance.
• NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284929.RAyjuLjXxRS7Pun2zzpsQSkSPcP8gku7SMkFlPOpX_znA130_provenance.
• NP284931.RA3FBDtOgCxPvrSfNzg-xS9jxyNpSKQIxczrxM9qFtqeQ130_assertion description "[Mutations in the genes that encode filamin-1, Lis1 and doublecortin are responsible for X-linked lissencephaly in man, whereas mutations in the genes that encode Cdk5, its activator p35 and the reelin-signaling pathway disturb migration and architectonic development in mice.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284931.RA3FBDtOgCxPvrSfNzg-xS9jxyNpSKQIxczrxM9qFtqeQ130_provenance.