Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_provenance.
- NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_assertion description "[The SOD2 homozygous variant genotype (Val/Val) was associated with a greater risk of pancreatic cancer (adjusted OR, 1.96; 95% CI, 1.0-3.8; P = .04).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_provenance.
- NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_assertion evidence source_evidence_literature NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_provenance.
- NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_assertion SIO_000772 18205184 NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_provenance.
- NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_assertion wasDerivedFrom befree-20140225 NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_provenance.
- NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_assertion wasGeneratedBy ECO_0000203 NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP811772.RARf2TSbVjCjpknBG20kmg_tMdT3UKeml8Wg3bbWPaUlY130_provenance.