Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B095fd240eafca2d32f339485b2d96668> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B095fd240eafca2d32f339485b2d96668 NCIT_P378 "NCI" @default.
- B095fd240eafca2d32f339485b2d96668 type Axiom @default.
- B095fd240eafca2d32f339485b2d96668 annotatedProperty IAO_0000115 @default.
- B095fd240eafca2d32f339485b2d96668 annotatedSource NCIT_C151901 @default.
- B095fd240eafca2d32f339485b2d96668 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.