Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_provenance.
- NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_assertion description "[The Val12Met SNP in ABCG2 was associated with stroke in both white (hazard ratio, 1.46; 90% CI, 1.05 to 2.03) and black (hazard ratio, 3.59; 90% CI, 1.11 to 11.6) participants of CHS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_provenance.
- NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_assertion evidence source_evidence_literature NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_provenance.
- NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_assertion SIO_000772 19023099 NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_provenance.
- NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_assertion wasDerivedFrom befree-20140225 NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_provenance.
- NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_assertion wasGeneratedBy ECO_0000203 NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP325392.RAXsTaodPHiy8YdsYZQr2XAP4FTBuT61tHyfnUbxR98SE130_provenance.