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- Bf7916846f121657ff75772be35df6e6e NCIT_P378 "NCI" @default.
- Bf7916846f121657ff75772be35df6e6e type Axiom @default.
- Bf7916846f121657ff75772be35df6e6e annotatedProperty IAO_0000115 @default.
- Bf7916846f121657ff75772be35df6e6e annotatedSource NCIT_C96522 @default.
- Bf7916846f121657ff75772be35df6e6e annotatedTarget "A molecular genetic abnormality that refers to the mutation of the BMPR1A (bone morphogenetic protein receptor, type 1A) gene on chromosome 10q22.3." @default.