Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_provenance.
- NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_assertion description "[There were 4.6% of cases and 3.8% of controls heterozygous for the factor V Leiden mutation (NS), and 1.3% of cases and 1.7% of controls heterozygous for the prothrombin mutation (NS).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_provenance.
- NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_assertion evidence source_evidence_literature NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_provenance.
- NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_assertion SIO_000772 15948766 NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_provenance.
- NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_assertion wasDerivedFrom befree-2016 NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_provenance.
- NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_assertion wasGeneratedBy ECO_0000203 NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_provenance.
- befree-2016 importedOn "2016-02-19" NP498873.RARyajk2jGP8a2mw9DAUcZohDS5887BbG6GZ27x1fxZUk130_provenance.