Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_provenance.
- NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_assertion description "[Our data suggest that the GPS[+] phenotype is accounted for by monoallelic variants in ABCA4 and unlikely by the well-established AMD risk-increasing alleles at CFH, ARMS2, and C3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_provenance.
- NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_assertion evidence source_evidence_literature NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_provenance.
- NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_assertion SIO_000772 22427542 NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_provenance.
- NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_assertion wasDerivedFrom befree-2016 NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_provenance.
- NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_assertion wasGeneratedBy ECO_0000203 NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_provenance.
- befree-2016 importedOn "2016-02-19" NP968624.RA0DhxHOEOYNeOJsUoXiiEylUC2v0Zz3MOZooGttUa5rk130_provenance.