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- source_evidence_literature type ECO_0000212 NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_provenance.
- NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_assertion description "[Despite the fact that the frequency of TMIE variants in our study subjects was low, we suggested that c.257G>A (p.R86Q) variant is a de novo and may be as a risk factor for the development of hearing loss in Taiwanese.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_provenance.
- NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_assertion evidence source_evidence_literature NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_provenance.
- NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_assertion SIO_000772 20206386 NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_provenance.
- NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_assertion wasDerivedFrom gad-20150221 NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_provenance.
- NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_assertion wasGeneratedBy ECO_0000203 NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_provenance.
- gad-20150221 importedOn "2015-02-21" NP166741.RAFP318tQ8CR_P5GFiWua-sku-81bsdOmZTbD9TEh9M24130_provenance.