Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_provenance.
- befree-2016 importedOn "2016-02-19" NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_provenance.
- NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_assertion wasGeneratedBy ECO_0000203 NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_provenance.
- NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_assertion wasDerivedFrom befree-2016 NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_provenance.
- NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_assertion SIO_000772 15841171 NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_provenance.
- NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_assertion evidence source_evidence_literature NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_provenance.
- NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_assertion description "[Rare mutations in MEF2A have been proposed as a cause of coronary artery disease (CAD) and myocardial infarction (MI).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490787.RA0wHfAMdV8_hFuMjRPVb9N07XOtFlAkzgr5FpUThAs7g130_provenance.