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- NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_assertion type Assertion NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_head.
- NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_assertion description "[In recent years, the identification of five different mutated genes in the mouse (Pax3, Mitf; Myo7a, Pou4f3, and Myo15) has led directly to the identification of mutations in families with either congenital sensorineural deafness or progressive sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_provenance.
- NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_assertion evidence source_evidence_literature NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_provenance.
- NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_assertion SIO_000772 10320095 NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_provenance.
- NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_assertion wasDerivedFrom befree-20150227 NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_provenance.
- NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_assertion wasGeneratedBy ECO_0000203 NP635826.RAKpINGwWNug-8Ysc42ORZaKsfhHTI5JzV5jbkLYSuBfM130_provenance.