Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_provenance.
- NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_assertion description "[A genetic risk score based on nine genetic variants independently associated with CAD irrespective of other cardiovascular risk factors was associated with the presence of the disease. Cohort studies are needed to determine whether this genetic risk score can improve the predictive capacity or the risk classification of classical risk functions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_provenance.
- NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_assertion evidence source_evidence_literature NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_provenance.
- NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_assertion SIO_000772 20738937 NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_provenance.
- NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_assertion wasDerivedFrom gad-20130706 NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_provenance.
- NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_assertion wasGeneratedBy ECO_0000203 NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_provenance.
- gad-20130706 importedOn "2013-07-06" NP77481.RA3xssYBelK8YnzyL6OzckJsd8x5LuM4rjimYMGmYcpsU130_provenance.