Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_assertion> ?p ?o ?g. }
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- NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_assertion type Assertion NP492134.RAJKIN3EBp7SP8FWPf_X0SoSEuWcMV_Lq2PBsO6OBkVtA130_head.
- 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.