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- Baab68d9f98081bcdb4ff8d938c875b57 NCIT_P378 "NCI" @default.
- Baab68d9f98081bcdb4ff8d938c875b57 type Axiom @default.
- Baab68d9f98081bcdb4ff8d938c875b57 annotatedProperty IAO_0000115 @default.
- Baab68d9f98081bcdb4ff8d938c875b57 annotatedSource NCIT_C200422 @default.
- Baab68d9f98081bcdb4ff8d938c875b57 annotatedTarget "An autosomal dominant inherited syndrome caused by germline mutations of the SAMD9L gene. It is characterized by cerebellar ataxia, cytopenia in all cell lineages, and predisposition to myelodysplasia and myeloid leukemia." @default.