Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_provenance.
- NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_assertion description "[The aim of the present study was to test for an association between the CFH-Y402H variant and MI in a large case-control sample with a familial background for CAD (coronary artery disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_provenance.
- NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_assertion evidence source_evidence_literature NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_provenance.
- NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_assertion SIO_000772 17472578 NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_provenance.
- NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_assertion wasDerivedFrom befree-20150227 NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_provenance.
- NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_assertion wasGeneratedBy ECO_0000203 NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP446598.RAPYQXtLsjUpOM6Lvaqal3Tci9ahGHvZuppAkBdt1OJs0130_provenance.