Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_provenance.
- NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_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." NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_provenance.
- NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_assertion evidence source_evidence_literature NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_provenance.
- NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_assertion SIO_000772 17721328 NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_provenance.
- NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_assertion wasDerivedFrom gad-20150221 NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_provenance.
- NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_assertion wasGeneratedBy ECO_0000203 NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_provenance.
- gad-20150221 importedOn "2015-02-21" NP111076.RAydVQonrxWO7GFytHMDQSL3NdkY2Z13p1lwgThuwFpaI130_provenance.