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- source_evidence_literature type ECO_0000212 NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_provenance.
- NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_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." NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_provenance.
- NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_assertion evidence source_evidence_literature NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_provenance.
- NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_assertion SIO_000772 12642359 NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_provenance.
- NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_assertion wasDerivedFrom befree-20150227 NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_provenance.
- NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_assertion wasGeneratedBy ECO_0000203 NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_provenance.
- befree-20150227 importedOn "2015-02-27" NP578811.RA1P6ggo17e4Xm2Pp8LOZ116jhRx-nD4XIpjRSIzGrMjs130_provenance.