Matches in Nanopublications for { ?s ?p "[A DNA coding variant (rs3736265) and a 3'UTR-resident regulatory variant (rs3774923) in PPARGC1A were independently associated with NV AMD (exact P = 0.003, both SNPs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP775068.RAs3e7JZ4gDY91ZzjxCPlXgsYfrvbxJb7-4BQMsa0JMPE130_assertion description "[A DNA coding variant (rs3736265) and a 3'UTR-resident regulatory variant (rs3774923) in PPARGC1A were independently associated with NV AMD (exact P = 0.003, both SNPs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP775068.RAs3e7JZ4gDY91ZzjxCPlXgsYfrvbxJb7-4BQMsa0JMPE130_provenance.
- NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_assertion description "[A DNA coding variant (rs3736265) and a 3'UTR-resident regulatory variant (rs3774923) in PPARGC1A were independently associated with NV AMD (exact P = 0.003, both SNPs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_provenance.
- NP432296.RAeNogEh3oI8TK3MLZLB2gu4XZ1Naje4Tr-BGdsy9-5aU130_assertion description "[A DNA coding variant (rs3736265) and a 3'UTR-resident regulatory variant (rs3774923) in PPARGC1A were independently associated with NV AMD (exact P = 0.003, both SNPs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432296.RAeNogEh3oI8TK3MLZLB2gu4XZ1Naje4Tr-BGdsy9-5aU130_provenance.