Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_provenance.
- NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_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." NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_provenance.
- NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_assertion evidence source_evidence_curated NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_provenance.
- NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_assertion SIO_000772 17721328 NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_provenance.
- NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_assertion wasDerivedFrom ctd_human-20150221 NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_provenance.
- NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_assertion wasGeneratedBy ECO_0000218 NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP14222.RAhehMRKQ7USKo6eYOi89fBMgKV876dvlh7RoE9LSeC6Q130_provenance.