Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_provenance.
- NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_assertion description "[Haplotype B in the ALOX5AP gene was associated with an increased risk of MI in the German population, confirming previously reported associations of this haplotype with CAD (coronary artery disease) in populations from Scotland and Italy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_provenance.
- NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_assertion evidence source_evidence_literature NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_provenance.
- NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_assertion SIO_000772 18318662 NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_provenance.
- NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_assertion wasDerivedFrom befree-20150227 NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_provenance.
- NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_assertion wasGeneratedBy ECO_0000203 NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP236421.RA8cr7jXUy0jGDhNvX7yCIuoar4AsDep4U8W9VppvUbUs130_provenance.