Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_provenance.
- NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_assertion description "[The multivariate analysis showed that the homozygosity for the eNOS 4a rare variant represented an independent predisposition factor to ACS (odds ratio [OR] 2.5, 95% CI 1.1-5.4, P =.02) and in particular influenced the risk of acute myocardial infarction (OR 3.6, 95% CI 1.2-11.5, P =.03).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_provenance.
- NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_assertion evidence source_evidence_literature NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_provenance.
- NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_assertion SIO_000772 14999203 NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_provenance.
- NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_assertion wasDerivedFrom befree-20140225 NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_provenance.
- NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_assertion wasGeneratedBy ECO_0000203 NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP478389.RAnvuGQSLP_DoLS3GqRVNy1DPpXqLBhqQHyDXNzFGIpeA130_provenance.