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- source_evidence_literature type ECO_0000212 NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_provenance.
- NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_assertion description "[Here, we show that mutations in the inwardly rectifying K(+) channel gene KCNJ10 are associated with nonsyndromic hearing loss in carriers of SLC26A4 mutations with an EVA/PS phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_provenance.
- NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_assertion evidence source_evidence_literature NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_provenance.
- NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_assertion SIO_000772 19426954 NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_provenance.
- NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_assertion wasDerivedFrom befree-2016 NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_provenance.
- NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_assertion wasGeneratedBy ECO_0000203 NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_provenance.
- befree-2016 importedOn "2016-02-19" NP737514.RA-OVaw3UO1MoA1emTGUpaNumO59UWMJIZvD_DRTXnJwU130_provenance.