Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B1093069851522fe5238096e5e4be598c> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B1093069851522fe5238096e5e4be598c NCIT_P378 "NCI" @default.
- B1093069851522fe5238096e5e4be598c type Axiom @default.
- B1093069851522fe5238096e5e4be598c annotatedProperty IAO_0000115 @default.
- B1093069851522fe5238096e5e4be598c annotatedSource NCIT_C13727 @default.
- B1093069851522fe5238096e5e4be598c annotatedTarget "A translocation between chromosomes 12 and 21 involved in TEL-AML1 oncogene formation. The translocation produces a chimeric gene encoding a protein consisting of the N-terminal HLH domain of the TEL ETS-like transcription factor fused with a nearly complete AML1 protein. t(12;21) is the most frequent translocation causing ALL, accounting for 20% of ALL cases." @default.