Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B444e73724bd599ae94b0aafc8fcbf007> ?p ?o ?g. }
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- B444e73724bd599ae94b0aafc8fcbf007 NCIT_P378 "NCI" @default.
- B444e73724bd599ae94b0aafc8fcbf007 type Axiom @default.
- B444e73724bd599ae94b0aafc8fcbf007 annotatedProperty IAO_0000115 @default.
- B444e73724bd599ae94b0aafc8fcbf007 annotatedSource NCIT_C176809 @default.
- B444e73724bd599ae94b0aafc8fcbf007 annotatedTarget "An autosomal recessive common variable immunodeficiency caused by mutation(s) in the LRBA gene, encoding lipopolysaccharide-responsive and beige-like anchor protein. It is characterized by recurrent infections and the development of autoimmune disorders." @default.