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- Bf44b0d6c6fac5beb4fc50bf9f0266e9d NCIT_P378 "NCI" @default.
- Bf44b0d6c6fac5beb4fc50bf9f0266e9d type Axiom @default.
- Bf44b0d6c6fac5beb4fc50bf9f0266e9d annotatedProperty IAO_0000115 @default.
- Bf44b0d6c6fac5beb4fc50bf9f0266e9d annotatedSource NCIT_C151901 @default.
- Bf44b0d6c6fac5beb4fc50bf9f0266e9d annotatedTarget "An autosomal dominant familial myelodysplastic syndrome/acute myeloid leukemia syndrome characterized by inherited mutations in the gene on chromosome 5 encoding the DEAD box RNA helicase DDX41. Patients usually present with leukopenia, hypocellular bone marrow with prominent erythroid dysplasia and a normal karyotype, often leading to erythroleukemia. The prognosis is generally poor. (WHO 2017)" @default.