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- NP306748.RAtWsmBaF6AlWrqJgD4_MqjqiA_JMgRHXEFEKD2w6KwcM130_assertion type Assertion NP306748.RAtWsmBaF6AlWrqJgD4_MqjqiA_JMgRHXEFEKD2w6KwcM130_head.
- NP306748.RAtWsmBaF6AlWrqJgD4_MqjqiA_JMgRHXEFEKD2w6KwcM130_assertion wasGeneratedBy ECO_0000203 NP306748.RAtWsmBaF6AlWrqJgD4_MqjqiA_JMgRHXEFEKD2w6KwcM130_provenance.
- NP306748.RAtWsmBaF6AlWrqJgD4_MqjqiA_JMgRHXEFEKD2w6KwcM130_assertion wasDerivedFrom befree-20140225 NP306748.RAtWsmBaF6AlWrqJgD4_MqjqiA_JMgRHXEFEKD2w6KwcM130_provenance.
- NP306748.RAtWsmBaF6AlWrqJgD4_MqjqiA_JMgRHXEFEKD2w6KwcM130_assertion SIO_000772 11683347 NP306748.RAtWsmBaF6AlWrqJgD4_MqjqiA_JMgRHXEFEKD2w6KwcM130_provenance.
- NP306748.RAtWsmBaF6AlWrqJgD4_MqjqiA_JMgRHXEFEKD2w6KwcM130_assertion evidence source_evidence_literature NP306748.RAtWsmBaF6AlWrqJgD4_MqjqiA_JMgRHXEFEKD2w6KwcM130_provenance.
- NP306748.RAtWsmBaF6AlWrqJgD4_MqjqiA_JMgRHXEFEKD2w6KwcM130_assertion description "[In this study, we genetically investigated the presence of EYA1 mutations in a BO syndrome family in which we observed congenital preauricular fistulae, branchial fistulae (cysts) and hearing loss in four generations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP306748.RAtWsmBaF6AlWrqJgD4_MqjqiA_JMgRHXEFEKD2w6KwcM130_provenance.