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- Bf5c2722e5055bf9baf91948f50ed8fca NCIT_P378 "NCI" @default.
- Bf5c2722e5055bf9baf91948f50ed8fca type Axiom @default.
- Bf5c2722e5055bf9baf91948f50ed8fca annotatedProperty IAO_0000115 @default.
- Bf5c2722e5055bf9baf91948f50ed8fca annotatedSource NCIT_C74996 @default.
- Bf5c2722e5055bf9baf91948f50ed8fca annotatedTarget "A rare genetic syndrome characterized by the hypoplasia or absence of the cerebellar vermis. Signs and symptoms include rapid breathing (hyperpnea), sleep apnea, abnormal eye movements, mental retardation, and ataxia." @default.