Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B009ae3dfbd673db7c68a8c7f0b59f110> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B009ae3dfbd673db7c68a8c7f0b59f110 NCIT_P378 "NCI" @default.
- B009ae3dfbd673db7c68a8c7f0b59f110 type Axiom @default.
- B009ae3dfbd673db7c68a8c7f0b59f110 annotatedProperty IAO_0000115 @default.
- B009ae3dfbd673db7c68a8c7f0b59f110 annotatedSource NCIT_C97569 @default.
- B009ae3dfbd673db7c68a8c7f0b59f110 annotatedTarget "Human HOXA11 wild-type allele is located in the vicinity of 7p15.2 and is approximately 4 kb in length. This allele, which encodes homeobox protein Hox-A11, plays a role in transcriptional regulation. Mutation of the gene is associated with radioulnar synostosis with amegakaryocytic thrombocytopenia. Two chromosomal aberrations inv(7)(p15q34) and t(7;7)(p15;q34) of this gene and the TCRB gene locus lead to ectopic expression of the HOXA11 gene and are associated with T-cell acute lymphoblastic leukemia. A chromosomal translocation t(7;11)(p15;p15) of this gene and the NUP98 gene might be associated with chronic myelogenous leukemia." @default.