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- B87dc734b54f3d7ec5736f95e30288e11 NCIT_P378 "NICHD" @default.
- B87dc734b54f3d7ec5736f95e30288e11 type Axiom @default.
- B87dc734b54f3d7ec5736f95e30288e11 annotatedProperty NCIT_P325 @default.
- B87dc734b54f3d7ec5736f95e30288e11 annotatedSource NCIT_C84646 @default.
- B87dc734b54f3d7ec5736f95e30288e11 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.