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- NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_assertion type Assertion NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_head.
- NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_assertion wasGeneratedBy ECO_0000218 NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_provenance.
- NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_assertion wasDerivedFrom uniprot-2016 NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_provenance.
- NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_assertion SIO_000772 10925378 NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_provenance.
- NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_assertion evidence source_evidence_curated NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_provenance.
- NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_assertion description "[Mutations in the KCNQ4 K+ channel gene, responsible for autosomal dominant hearing loss, cluster in the channel pore region.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP936.RAPA6ZLzhRot6fK7vGNDxbsyNnxmbBrqagmo5NowGOW-o130_provenance.