Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_provenance.
- NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_assertion description "[Independent analyses showed the PSEL 290NN genotype to be a significant predictor of CHD in whites (HRR 1.30, 95%CI 1.00-1.70, P=0.05).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_provenance.
- NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_assertion evidence source_evidence_literature NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_provenance.
- NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_assertion SIO_000772 17420019 NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_provenance.
- NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_assertion wasDerivedFrom befree-20140225 NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_provenance.
- NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_assertion wasGeneratedBy ECO_0000203 NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP432928.RAYpfo-FUYb19s1_WrMgerZGHHTjbgoIyJScN8kh3Kukg130_provenance.