Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_provenance.
- NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_assertion description "[Carriers of the -5C allele were significantly over-represented in the group of patients developing acute coronary syndromes (relative risk [RR] 1.43, 95% confidence interval [CI] 1.05 to 1.95, p = 0.02).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_provenance.
- NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_assertion evidence source_evidence_literature NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_provenance.
- NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_assertion SIO_000772 11583876 NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_provenance.
- NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_assertion wasDerivedFrom befree-20140225 NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_provenance.
- NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_assertion wasGeneratedBy ECO_0000203 NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP220073.RA91gNgksxAFhNLktJPyWLf5CCFphNVLqxnPVOnbmojLM130_provenance.