Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B19d34048943a722643f131f823e68dd7> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B19d34048943a722643f131f823e68dd7 NCIT_P378 "NCI" @default.
- B19d34048943a722643f131f823e68dd7 type Axiom @default.
- B19d34048943a722643f131f823e68dd7 annotatedProperty IAO_0000115 @default.
- B19d34048943a722643f131f823e68dd7 annotatedSource NCIT_C3895 @default.
- B19d34048943a722643f131f823e68dd7 annotatedTarget "A hereditary immunodeficiency disorder caused by the lack of expression of major histocompatibility complex (MHC) proteins. Signs include upper and lower respiratory tract bacterial infections, malabsorption, diarrhea, and mucocutaneous candidiasis." @default.