Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B18e87c9e902157fc1c9e5126c690104e> ?p ?o ?g. }
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- B18e87c9e902157fc1c9e5126c690104e hasDbXref "PMID:33231617" @default.
- B18e87c9e902157fc1c9e5126c690104e hasDbXref "https://orcid.org/0000-0001-5208-3432" @default.
- B18e87c9e902157fc1c9e5126c690104e hasDbXref "https://orcid.org/0000-0002-7371-8158" @default.
- B18e87c9e902157fc1c9e5126c690104e hasDbXref "https://orcid.org/0000-0003-0113-912X" @default.
- B18e87c9e902157fc1c9e5126c690104e type Axiom @default.
- B18e87c9e902157fc1c9e5126c690104e annotatedProperty IAO_0000115 @default.
- B18e87c9e902157fc1c9e5126c690104e annotatedSource MONDO_0030302 @default.
- B18e87c9e902157fc1c9e5126c690104e annotatedTarget "A human immunodeficiency characterized by early-onset life-threatening infections, combined T and B cell immunodeficiency, severe neutrophil defects, and impaired platelet aggregation, caused by a variation in the SLP76 gene." @default.