Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bfe4d38e7ce4f6f48ce3107868e3876ef> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bfe4d38e7ce4f6f48ce3107868e3876ef NCIT_P378 "NCI" @default.
- Bfe4d38e7ce4f6f48ce3107868e3876ef type Axiom @default.
- Bfe4d38e7ce4f6f48ce3107868e3876ef annotatedProperty IAO_0000115 @default.
- Bfe4d38e7ce4f6f48ce3107868e3876ef annotatedSource NCIT_C5402 @default.
- Bfe4d38e7ce4f6f48ce3107868e3876ef annotatedTarget "A medulloblastoma characterized by the loss of one of the p13 regions of chromosome 17. Loss of genetic material of chromosome arm 17p is the most common molecular genetic abnormality found in medulloblastomas." @default.