Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_provenance.
- NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_assertion description "[This is the first report of a CAD association signal in a population of African ancestry with a common variant within the CDKN2B gene, independent from previous findings in European and East Asian ancestry populations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_provenance.
- NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_assertion evidence source_evidence_literature NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_provenance.
- NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_assertion SIO_000772 21270820 NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_provenance.
- NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_assertion wasDerivedFrom befree-20140225 NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_provenance.
- NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_assertion wasGeneratedBy ECO_0000203 NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP740076.RA7WTIAvpWtP9HTG8W6BbYV5oklHuNfTkP4ziE3HQwfJE130_provenance.