Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_assertion> ?p ?o ?g. }
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- NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_assertion type Assertion NP254335.RAQPFOgFEniPJg72vxyWRbGcRQL0wEk7v8de6adgrLJuI130_head.
- 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.