Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_provenance.
- NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_assertion description "[The results of this study indicate that the 9p21 variation has an impact on CDKN2A and CDKN2B expression in VSMCs and influences VMSC proliferation, which likely represents an important mechanism for the association between this genetic locus and susceptibility to CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_provenance.
- NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_assertion evidence source_evidence_literature NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_provenance.
- NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_assertion SIO_000772 22706276 NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_provenance.
- NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_assertion wasDerivedFrom befree-20150227 NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_provenance.
- NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_assertion wasGeneratedBy ECO_0000203 NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP306836.RAfLi_Gw4cXSVH9oI460fR_x1rUia6sby165qwDjHLToY130_provenance.