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- B6f48d9b015f8297450217ad06b19e48e NCIT_P378 "NCI" @default.
- B6f48d9b015f8297450217ad06b19e48e type Axiom @default.
- B6f48d9b015f8297450217ad06b19e48e annotatedProperty IAO_0000115 @default.
- B6f48d9b015f8297450217ad06b19e48e annotatedSource NCIT_C176908 @default.
- B6f48d9b015f8297450217ad06b19e48e annotatedTarget "An inherited condition caused by autosomal dominant mutation(s) in the SAMD9L gene, encoding sterile alpha motif domain-containing protein 9-like. The condition is characterized by an increased risk of developing myelodysplastic syndrome and acute myelogenous leukemia." @default.