Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bbb66fd6f72c0caaa59d1240058804ce5> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Bbb66fd6f72c0caaa59d1240058804ce5 NCIT_P378 "NICHD" @default.
- Bbb66fd6f72c0caaa59d1240058804ce5 type Axiom @default.
- Bbb66fd6f72c0caaa59d1240058804ce5 annotatedProperty NCIT_P325 @default.
- Bbb66fd6f72c0caaa59d1240058804ce5 annotatedSource NCIT_C2941 @default.
- Bbb66fd6f72c0caaa59d1240058804ce5 annotatedTarget "An autosomal recessive syndrome characterized by immune deficiency, partial oculocutaneous albinism, a bleeding disorder due to deficient platelet dense bodies, neutropenia, neutrophils with impaired chemotaxis and bactericidal activity, recurrent infection, and abnormal natural killer (NK) cell function." @default.