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- NP990946.RAeTkrDih__VAw0gyWOccLRW8A2SUH9MXJWo-HBonMh9o130_assertion type Assertion NP990946.RAeTkrDih__VAw0gyWOccLRW8A2SUH9MXJWo-HBonMh9o130_head.
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- NP990946.RAeTkrDih__VAw0gyWOccLRW8A2SUH9MXJWo-HBonMh9o130_assertion wasDerivedFrom befree-20150227 NP990946.RAeTkrDih__VAw0gyWOccLRW8A2SUH9MXJWo-HBonMh9o130_provenance.
- NP990946.RAeTkrDih__VAw0gyWOccLRW8A2SUH9MXJWo-HBonMh9o130_assertion SIO_000772 11020419 NP990946.RAeTkrDih__VAw0gyWOccLRW8A2SUH9MXJWo-HBonMh9o130_provenance.
- NP990946.RAeTkrDih__VAw0gyWOccLRW8A2SUH9MXJWo-HBonMh9o130_assertion evidence source_evidence_literature NP990946.RAeTkrDih__VAw0gyWOccLRW8A2SUH9MXJWo-HBonMh9o130_provenance.
- NP990946.RAeTkrDih__VAw0gyWOccLRW8A2SUH9MXJWo-HBonMh9o130_assertion description "[Novel mutation in RP2 gene in two brothers with X-linked retinitis pigmentosa and mtDNA mutation of leber hereditary optic neuropathy who showed marked differences in clinical severity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP990946.RAeTkrDih__VAw0gyWOccLRW8A2SUH9MXJWo-HBonMh9o130_provenance.