Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_provenance.
- NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_assertion description "[We determined the prevalence of the G20210A mutation and prothrombin activity in 660 individuals, of whom 436 had angiographically documented severe coronary artery disease (CAD patients) and 224 had normal coronary angiography (CAD-free control subjects).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_provenance.
- NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_assertion evidence source_evidence_literature NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_provenance.
- NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_assertion SIO_000772 11369682 NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_provenance.
- NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_assertion wasDerivedFrom befree-2016 NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_provenance.
- NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_assertion wasGeneratedBy ECO_0000203 NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_provenance.
- befree-2016 importedOn "2016-02-19" NP318703.RAD5wbRDWd0-9ekDLscw7MJCO78fVfxHW4vQPT3SsAPpA130_provenance.