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- Bbe474a0d86b39fe74f974b19a1388a8e NCIT_P378 "NCI" @default.
- Bbe474a0d86b39fe74f974b19a1388a8e type Axiom @default.
- Bbe474a0d86b39fe74f974b19a1388a8e annotatedProperty IAO_0000115 @default.
- Bbe474a0d86b39fe74f974b19a1388a8e annotatedSource NCIT_C84646 @default.
- Bbe474a0d86b39fe74f974b19a1388a8e annotatedTarget "A rare group of disorders that result in anemia that is caused by ineffective erythropoiesis, which is associated with multinuclear erythroblasts, and which may present in childhood. The most common mutations are in the CDAN1 and SEC23B genes." @default.