Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_provenance.
- NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_assertion description "[Factor V Leiden (a point mutation [1691G-->A] in the factor V gene), the prothrombin 20210G-->A mutation, and homozygosity for a common polymorphism in the methylene tetrahydrofolate reductase (MTHFR) gene (677C-->T) have been associated with arterial and venous thrombosis and arterial occlusive disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_provenance.
- NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_assertion evidence source_evidence_literature NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_provenance.
- NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_assertion SIO_000772 10360908 NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_provenance.
- NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_assertion wasDerivedFrom befree-2016 NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_provenance.
- NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_assertion wasGeneratedBy ECO_0000203 NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_provenance.
- befree-2016 importedOn "2016-02-19" NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_provenance.