Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B5e657c6cd5f03a0359d7347c5b90818b> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B5e657c6cd5f03a0359d7347c5b90818b NCIT_P378 "NCI" @default.
- B5e657c6cd5f03a0359d7347c5b90818b type Axiom @default.
- B5e657c6cd5f03a0359d7347c5b90818b annotatedProperty IAO_0000115 @default.
- B5e657c6cd5f03a0359d7347c5b90818b annotatedSource NCIT_C176809 @default.
- B5e657c6cd5f03a0359d7347c5b90818b 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.