Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_provenance.
- NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_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." NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_provenance.
- NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_assertion evidence source_evidence_literature NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_provenance.
- NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_assertion SIO_000772 10360908 NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_provenance.
- NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_assertion wasDerivedFrom befree-2016 NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_provenance.
- NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_assertion wasGeneratedBy ECO_0000203 NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_provenance.
- befree-2016 importedOn "2016-02-19" NP254333.RApDEnvz0qOzZDO6s_y2XsNv-BYLCOqibq_UNP2sLnVuY130_provenance.