Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bc2d422fb43af950acdc61cb16df8a767> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bc2d422fb43af950acdc61cb16df8a767 NCIT_P378 "NCI" @default.
- Bc2d422fb43af950acdc61cb16df8a767 type Axiom @default.
- Bc2d422fb43af950acdc61cb16df8a767 annotatedProperty IAO_0000115 @default.
- Bc2d422fb43af950acdc61cb16df8a767 annotatedSource NCIT_C99295 @default.
- Bc2d422fb43af950acdc61cb16df8a767 annotatedTarget "A fusion gene (~5.9 kb) that results from a chromosomal translocation t(3;21)(q26;q22) which fuses the first 5 exons of the RUNX1 gene to most of the MECOM gene. This rearrangement is associated with acute myelogenous leukemia, chronic myelogenous leukemia and myelodysplasic syndrome." @default.