Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B96c67009f47e5f508d888ce1d49c2242> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B96c67009f47e5f508d888ce1d49c2242 NCIT_P378 "NCI" @default.
- B96c67009f47e5f508d888ce1d49c2242 type Axiom @default.
- B96c67009f47e5f508d888ce1d49c2242 annotatedProperty IAO_0000115 @default.
- B96c67009f47e5f508d888ce1d49c2242 annotatedSource NCIT_C132102 @default.
- B96c67009f47e5f508d888ce1d49c2242 annotatedTarget "A cytogenetic abnormality that refers to the translocation of chromosome 10p12 with chromosome 11q23. It is associated with acute myeloid leukemia in childhood." @default.