Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_provenance.
- NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_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." NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_provenance.
- NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_assertion evidence source_evidence_literature NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_provenance.
- NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_assertion SIO_000772 21270820 NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_provenance.
- NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_assertion wasDerivedFrom befree-20140225 NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_provenance.
- NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_assertion wasGeneratedBy ECO_0000203 NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP688044.RA0-AjBmd4PWfQbi_m-OuEXX6YdPyjXNhbxAFo3g7pIrQ130_provenance.