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- source_evidence_literature type ECO_0000212 NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_provenance.
- NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_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." NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_provenance.
- NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_assertion evidence source_evidence_literature NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_provenance.
- NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_assertion SIO_000772 15861005 NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_provenance.
- NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_assertion wasDerivedFrom befree-2016 NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_provenance.
- NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_assertion wasGeneratedBy ECO_0000203 NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_provenance.
- befree-2016 importedOn "2016-02-19" NP492142.RA0eP-q75k5fd-EEwB47yP2qk7NSDcqR9PdKv8_Tjctw4130_provenance.