Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B97997774ab79e9e8e07ee89d50373d16> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- B97997774ab79e9e8e07ee89d50373d16 NCIT_P383 "SY" @default.
- B97997774ab79e9e8e07ee89d50373d16 NCIT_P384 "NCI" @default.
- B97997774ab79e9e8e07ee89d50373d16 type Axiom @default.
- B97997774ab79e9e8e07ee89d50373d16 annotatedProperty hasExactSynonym @default.
- B97997774ab79e9e8e07ee89d50373d16 annotatedSource NCIT_C131806 @default.
- B97997774ab79e9e8e07ee89d50373d16 annotatedTarget "Nijmegen Breakage Syndrome 1 Gene Mutation" @default.