Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_provenance.
- NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_assertion description "[The K allele of the R219K variant was significantly more frequent in FH subjects without premature CHD (0.32, 95% CI 0.27 to 0.37) than in FH subjects with premature CHD (0.25, 95% CI 0.21 to 0.29) (p<0.05), suggesting that the genetic variant R219K in ABCA1 could influence the development and progression of atherosclerosis in FH subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_provenance.
- NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_assertion evidence source_evidence_literature NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_provenance.
- NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_assertion SIO_000772 12624133 NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_provenance.
- NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_assertion wasDerivedFrom befree-20140225 NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_provenance.
- NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_assertion wasGeneratedBy ECO_0000203 NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP294901.RAt0jiyAn0yxsvT2jAikDIIRMymaCtKmn4Pe3LI3LccEA130_provenance.