Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Baa6f450353efebc7862cb3f0f3c29a1e> ?p ?o ?g. }
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- Baa6f450353efebc7862cb3f0f3c29a1e hasDbXref "https://orcid.org/0000-0002-0736-9199" @default.
- Baa6f450353efebc7862cb3f0f3c29a1e type Axiom @default.
- Baa6f450353efebc7862cb3f0f3c29a1e annotatedProperty IAO_0000115 @default.
- Baa6f450353efebc7862cb3f0f3c29a1e annotatedSource MONDO_0100191 @default.
- Baa6f450353efebc7862cb3f0f3c29a1e annotatedTarget "A heterogeneous group of genetic conditions, with Mendelian (autosomal dominant, recessive, or X-linked) or chromosomal etiology that are characterized by abnormalities in the kidney or urinary system." @default.