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- NP902767.RAapkoaqv5jc0cR5B1g5J-2HMODinnjUbnMC0zl8mKSp0130_assertion type Assertion NP902767.RAapkoaqv5jc0cR5B1g5J-2HMODinnjUbnMC0zl8mKSp0130_head.
- NP902767.RAapkoaqv5jc0cR5B1g5J-2HMODinnjUbnMC0zl8mKSp0130_assertion description "[Novel mutations of MYO15A associated with profound deafness in consanguineous families and moderately severe hearing loss in a patient with Smith-Magenis syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP902767.RAapkoaqv5jc0cR5B1g5J-2HMODinnjUbnMC0zl8mKSp0130_provenance.
- NP902767.RAapkoaqv5jc0cR5B1g5J-2HMODinnjUbnMC0zl8mKSp0130_assertion evidence source_evidence_literature NP902767.RAapkoaqv5jc0cR5B1g5J-2HMODinnjUbnMC0zl8mKSp0130_provenance.
- NP902767.RAapkoaqv5jc0cR5B1g5J-2HMODinnjUbnMC0zl8mKSp0130_assertion SIO_000772 11735029 NP902767.RAapkoaqv5jc0cR5B1g5J-2HMODinnjUbnMC0zl8mKSp0130_provenance.
- NP902767.RAapkoaqv5jc0cR5B1g5J-2HMODinnjUbnMC0zl8mKSp0130_assertion wasDerivedFrom befree-20150227 NP902767.RAapkoaqv5jc0cR5B1g5J-2HMODinnjUbnMC0zl8mKSp0130_provenance.
- NP902767.RAapkoaqv5jc0cR5B1g5J-2HMODinnjUbnMC0zl8mKSp0130_assertion wasGeneratedBy ECO_0000203 NP902767.RAapkoaqv5jc0cR5B1g5J-2HMODinnjUbnMC0zl8mKSp0130_provenance.