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- source_evidence_literature type ECO_0000212 NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_provenance.
- NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_assertion description "[Based on the studies in mice, we have screened DNA from human families and identified a nonsense mutation in the human ortholog of the murine Comt2 gene that causes nonsyndromic deafness.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_provenance.
- NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_assertion evidence source_evidence_literature NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_provenance.
- NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_assertion SIO_000772 18794526 NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_provenance.
- NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_assertion wasDerivedFrom befree-2016 NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_provenance.
- NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_assertion wasGeneratedBy ECO_0000203 NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_provenance.
- befree-2016 importedOn "2016-02-19" NP693317.RA47DuvQCRSVmx0DkgeH0bGB1zgpi7V7nkeQy1-br5R5U130_provenance.