Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bf8043d0e94a3c7fd83a729fe52f61bf1> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bf8043d0e94a3c7fd83a729fe52f61bf1 hasDbXref "NCIT:P378" @default.
- Bf8043d0e94a3c7fd83a729fe52f61bf1 type Axiom @default.
- Bf8043d0e94a3c7fd83a729fe52f61bf1 annotatedProperty IAO_0000115 @default.
- Bf8043d0e94a3c7fd83a729fe52f61bf1 annotatedSource MONDO_0010068 @default.
- Bf8043d0e94a3c7fd83a729fe52f61bf1 annotatedTarget "A rare genetic disorder characterized by bone marrow failure, spinal abnormalities, saddle nose, and metaphysical striation." @default.