Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP723884.RAbp8gbekpXvCYZaJOSkulD8SoTdLj9isWd-yx-VA5B5s130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723884.RAbp8gbekpXvCYZaJOSkulD8SoTdLj9isWd-yx-VA5B5s130_provenance.
• NP293629.RAVQhMOIRUNnl6jTcYnx2LG4cylH0Ime7H8ROpTQp5Sv8130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP293629.RAVQhMOIRUNnl6jTcYnx2LG4cylH0Ime7H8ROpTQp5Sv8130_provenance.
• NP598122.RAwEb9LZMUej8pU0JgE5jaoXg6ia1R4YnArXVKkxQ1R4I130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP598122.RAwEb9LZMUej8pU0JgE5jaoXg6ia1R4YnArXVKkxQ1R4I130_provenance.
• assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP382190.RAf5tGM8zuEZtcJP9k-Vx74Gmr808fH53aokQM7MZbJYk130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382190.RAf5tGM8zuEZtcJP9k-Vx74Gmr808fH53aokQM7MZbJYk130_provenance.
• NP852874.RA0soBtPlVktDW40Isb97c4JcMYqhLbuy9ZnPVbNPkNO4130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852874.RA0soBtPlVktDW40Isb97c4JcMYqhLbuy9ZnPVbNPkNO4130_provenance.
• NP600246.RALfxTXdo6SULZOwqgYdm72DSXg7jDO6D74tqXdmd_eQk130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP600246.RALfxTXdo6SULZOwqgYdm72DSXg7jDO6D74tqXdmd_eQk130_provenance.
• NP992078.RAX-iAP0FunP17NezOuiY6T9h3gj5RofyotN7LK7pMSC4130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP992078.RAX-iAP0FunP17NezOuiY6T9h3gj5RofyotN7LK7pMSC4130_provenance.
• NP992144.RAUewtclkz7W1M-OW-qGV69r8eVGY1OF3_W1642k_3LJI130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP992144.RAUewtclkz7W1M-OW-qGV69r8eVGY1OF3_W1642k_3LJI130_provenance.
• NP992134.RADgDYlUh2GLhL3qtLgHAFT7zZ8yCrrbdNKCz-82jJS8U130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP992134.RADgDYlUh2GLhL3qtLgHAFT7zZ8yCrrbdNKCz-82jJS8U130_provenance.
• assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• NP895128.RAXTGSDN6Nrpo5_6zOhJn75BNPOE1Dv-vxZUfhzU4f188130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895128.RAXTGSDN6Nrpo5_6zOhJn75BNPOE1Dv-vxZUfhzU4f188130_provenance.
• NP895129.RAYtNOc4zyhQ0ZrW0M7hnvhdK7eI5PLPO6yoCnzr4lUVI130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895129.RAYtNOc4zyhQ0ZrW0M7hnvhdK7eI5PLPO6yoCnzr4lUVI130_provenance.
• NP382227.RAtOv7bZKj9T9IphIWw75kNZYjnkpyoCqTRm0SJnuCnlw130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP382227.RAtOv7bZKj9T9IphIWw75kNZYjnkpyoCqTRm0SJnuCnlw130_provenance.
• NP895127.RACaeJndLN02EgVLiYqZ5P5Y7fVf3pB0Fh9HhiJ_EcF6M130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895127.RACaeJndLN02EgVLiYqZ5P5Y7fVf3pB0Fh9HhiJ_EcF6M130_provenance.
• NP381818.RApOBQ_Z_zSqJQD1OwZ3D5tKCmCIewPuwabhxi3dv24n4130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP381818.RApOBQ_Z_zSqJQD1OwZ3D5tKCmCIewPuwabhxi3dv24n4130_provenance.
• NP895130.RAmFGJA3Fh9WGLrsUtXfI8NYcaBiJ-TgxUcW0tnmAtLzo130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895130.RAmFGJA3Fh9WGLrsUtXfI8NYcaBiJ-TgxUcW0tnmAtLzo130_provenance.
• NP872725.RAKqhbJp0Mp0U4bsCSVfaLwOhWvMavpdaT4SjvfLK3fU4130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872725.RAKqhbJp0Mp0U4bsCSVfaLwOhWvMavpdaT4SjvfLK3fU4130_provenance.
• NP992092.RAMqJDv3JlhPl3NwFdTW8-CY848x5h5dl7Bm0byXi8hqU130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP992092.RAMqJDv3JlhPl3NwFdTW8-CY848x5h5dl7Bm0byXi8hqU130_provenance.
• NP992072.RA1Gz2oTdD8-rVnMYHMCPWIpJUrWoYc7ezVs2HLYzukd4130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP992072.RA1Gz2oTdD8-rVnMYHMCPWIpJUrWoYc7ezVs2HLYzukd4130_provenance.
• NP992107.RA0zMGGBPTOuE6cSDsWdGAgkZ1m77x3dzXFfaYHAthyO0130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP992107.RA0zMGGBPTOuE6cSDsWdGAgkZ1m77x3dzXFfaYHAthyO0130_provenance.
• NP895126.RA3_QXIM5qziYNkJms1qatxjK-rJYkZSWP-jsGXpUW9c0130_assertion description "[Mutations in three of the subunits, XPB, XPD and TTDA, lead to three distinct genetic disorders: xeroderma pigmentosum (XP), Cockayne syndrome (CS) and trichothiodystrophy (TTD) predisposing patients not only to cancer and ageing but also to developmental and neurological defects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP895126.RA3_QXIM5qziYNkJms1qatxjK-rJYkZSWP-jsGXpUW9c0130_provenance.