Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B692a98e8d428b6a9b574554d85fc2eac> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B692a98e8d428b6a9b574554d85fc2eac NCIT_P378 "NCI" @default.
- B692a98e8d428b6a9b574554d85fc2eac type Axiom @default.
- B692a98e8d428b6a9b574554d85fc2eac annotatedProperty IAO_0000115 @default.
- B692a98e8d428b6a9b574554d85fc2eac annotatedSource NCIT_C171624 @default.
- B692a98e8d428b6a9b574554d85fc2eac annotatedTarget "A cytogenetic abnormality that refers to any loss of genetic material from the short arm of chromosome 12 that includes the band at 12p13.2." @default.