Matches in Nanopublications for { ?s ?p "[The majority of the somatic mutations identified were identical to germline activating mutations in FGFR2 and FGFR3 that cause Apert Syndrome, Beare-Stevenson Syndrome, hypochondroplasia, achondroplasia and SADDAN syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP329582.RAdWl040PIYpYtid7cu9VYtKNXIdjBzGWIe4WJgyD_GVI130_assertion description "[The majority of the somatic mutations identified were identical to germline activating mutations in FGFR2 and FGFR3 that cause Apert Syndrome, Beare-Stevenson Syndrome, hypochondroplasia, achondroplasia and SADDAN syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP329582.RAdWl040PIYpYtid7cu9VYtKNXIdjBzGWIe4WJgyD_GVI130_provenance.
- NP872267.RAtVvjLoH_lK2n0DLH5byjiouZUWRlWUQa5rAgNa93Lqo130_assertion description "[The majority of the somatic mutations identified were identical to germline activating mutations in FGFR2 and FGFR3 that cause Apert Syndrome, Beare-Stevenson Syndrome, hypochondroplasia, achondroplasia and SADDAN syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP872267.RAtVvjLoH_lK2n0DLH5byjiouZUWRlWUQa5rAgNa93Lqo130_provenance.
- assertion description "[The majority of the somatic mutations identified were identical to germline activating mutations in FGFR2 and FGFR3 that cause Apert Syndrome, Beare-Stevenson Syndrome, hypochondroplasia, achondroplasia and SADDAN syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_assertion description "[The majority of the somatic mutations identified were identical to germline activating mutations in FGFR2 and FGFR3 that cause Apert Syndrome, Beare-Stevenson Syndrome, hypochondroplasia, achondroplasia and SADDAN syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588915.RAIxg_4EbE13U_4S9tvGOPV9Pbe6fmxiWoYTm1cBJuQS8130_provenance.
- NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_assertion description "[The majority of the somatic mutations identified were identical to germline activating mutations in FGFR2 and FGFR3 that cause Apert Syndrome, Beare-Stevenson Syndrome, hypochondroplasia, achondroplasia and SADDAN syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP400794.RA0j0k-GdJWuDTlWydHMsbKMtiy2xW9TvrGeUFSS-F-Bo130_provenance.
- NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_assertion description "[The majority of the somatic mutations identified were identical to germline activating mutations in FGFR2 and FGFR3 that cause Apert Syndrome, Beare-Stevenson Syndrome, hypochondroplasia, achondroplasia and SADDAN syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP611789.RA7TJUKGaJ_6qKKOTgCcCZPbB2SfRcDYvSGppWNniGBYk130_provenance.