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- source_evidence_literature type ECO_0000212 NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_provenance.
- NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_assertion description "[The family also was screened for mutations in cadherin 23, which accentuated hearing loss in a previously described human family with a PMCA2 mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_provenance.
- NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_assertion evidence source_evidence_literature NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_provenance.
- NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_assertion SIO_000772 17234811 NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_provenance.
- NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_assertion wasDerivedFrom befree-2016 NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_provenance.
- NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_assertion wasGeneratedBy ECO_0000203 NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_provenance.
- befree-2016 importedOn "2016-02-19" NP589536.RAB1fLzVyrPWk3ztfUuhRYGr3cRgPbbu30WCJ_0fh1-5M130_provenance.