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- source_evidence_literature type ECO_0000212 NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_provenance.
- NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_assertion description "[MLP is therefore a candidate gene for heritable forms of hypertrophic cardiomyopathy (HCM) and DCM in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_provenance.
- NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_assertion evidence source_evidence_literature NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_provenance.
- NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_assertion SIO_000772 12642359 NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_provenance.
- NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_assertion wasDerivedFrom befree-2016 NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_provenance.
- NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_assertion wasGeneratedBy ECO_0000203 NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_provenance.
- befree-2016 importedOn "2016-02-19" NP387307.RAcp9CP076j4DEzAbkfnFNg0hB3XH-gOtF2g3EoHPE3Os130_provenance.