Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_assertion> ?p ?o ?g. }
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- NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_assertion type Assertion NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_head.
- 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.
- NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_assertion evidence source_evidence_literature NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_provenance.
- NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_assertion SIO_000772 23335958 NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_provenance.
- NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_assertion wasDerivedFrom befree-20140225 NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_provenance.
- NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_assertion wasGeneratedBy ECO_0000203 NP500374.RABJmryTbMifOMOhSAdGw5JYGLl1IPuoBYZ0A4J-sOUP0130_provenance.