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- Be8bb91c2e4f483e9eee27f281c0f1a27 hasDbXref "NCIT:C84577" @default.
- Be8bb91c2e4f483e9eee27f281c0f1a27 type Axiom @default.
- Be8bb91c2e4f483e9eee27f281c0f1a27 annotatedProperty IAO_0000115 @default.
- Be8bb91c2e4f483e9eee27f281c0f1a27 annotatedSource MONDO_0020250 @default.
- Be8bb91c2e4f483e9eee27f281c0f1a27 annotatedTarget "An autosomal dominant hereditary condition characterized by optic atrophy and progressive visual loss." @default.