Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bf0f1a05e371cc8f3820f6c387eba2b42> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bf0f1a05e371cc8f3820f6c387eba2b42 NCIT_P378 "NICHD" @default.
- Bf0f1a05e371cc8f3820f6c387eba2b42 type Axiom @default.
- Bf0f1a05e371cc8f3820f6c387eba2b42 annotatedProperty NCIT_P325 @default.
- Bf0f1a05e371cc8f3820f6c387eba2b42 annotatedSource NCIT_C35710 @default.
- Bf0f1a05e371cc8f3820f6c387eba2b42 annotatedTarget "An autosomal recessive condition caused by mutation(s) in the AAAS gene encoding the protein ALADIN, and characterized by primary adrenal insufficiency, esophageal dysmotility, and absence of tear production." @default.