Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_provenance.
- NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_assertion description "[The MEF2A mutations may account for up to 1.93% of the disease population; thus, genetic testing based on mutational analysis of MEF2A may soon be available for many coronary artery disease/myocardial infarction patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_provenance.
- NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_assertion evidence source_evidence_literature NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_provenance.
- NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_assertion SIO_000772 15861005 NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_provenance.
- NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_assertion wasDerivedFrom befree-2016 NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_provenance.
- NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_assertion wasGeneratedBy ECO_0000203 NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_provenance.
- befree-2016 importedOn "2016-02-19" NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_provenance.