Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bc7a8b3c407022bfad36f8399f0a6b7bb> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bc7a8b3c407022bfad36f8399f0a6b7bb hasDbXref "NCIT:P378" @default.
- Bc7a8b3c407022bfad36f8399f0a6b7bb type Axiom @default.
- Bc7a8b3c407022bfad36f8399f0a6b7bb annotatedProperty IAO_0000115 @default.
- Bc7a8b3c407022bfad36f8399f0a6b7bb annotatedSource MONDO_0001734 @default.
- Bc7a8b3c407022bfad36f8399f0a6b7bb annotatedTarget "Hereditary disease characterized by seizures, mental retardation, developmental delay, and skin and ocular lesions. First signs usually occur during infancy or childhood but in rare cases may not occur until 2nd or 3rd decade." @default.