Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_provenance.
- NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_assertion description "[A myocyte enhancer factor 2A (MEF2A) mutation that segregated with coronary artery disease/myocardial infarction (CAD/MI) in a large family has recently been described.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_provenance.
- NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_assertion evidence source_evidence_literature NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_provenance.
- NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_assertion SIO_000772 15958500 NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_provenance.
- NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_assertion wasDerivedFrom befree-2016 NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_provenance.
- NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_assertion wasGeneratedBy ECO_0000203 NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_provenance.
- befree-2016 importedOn "2016-02-19" NP499636.RAawZPg1eGcSlrjk4mKCO6PKxcRBhQJCv937cRl7F_ef0130_provenance.