Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_provenance.
- NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_assertion description "[CYP2C9 and VKORC1 genetic polymorphism analysis might be necessary in patients with Factor V Leiden and prothrombin gene G2021A mutation(s).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_provenance.
- NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_assertion evidence source_evidence_literature NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_provenance.
- NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_assertion SIO_000772 17721328 NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_provenance.
- NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_assertion wasDerivedFrom gad-20130706 NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_provenance.
- NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_assertion wasGeneratedBy ECO_0000203 NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_provenance.
- gad-20130706 importedOn "2013-07-06" NP88215.RA_oPFgvBGh76Plx63zaL16S5CJ0qwkMGpJo7IhnGoUpY130_provenance.