Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B13e2922594e62db2c8a5ab9f589a0613> ?p ?o ?g. }
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- B13e2922594e62db2c8a5ab9f589a0613 hasDbXref "NCIT:C34842" @default.
- B13e2922594e62db2c8a5ab9f589a0613 type Axiom @default.
- B13e2922594e62db2c8a5ab9f589a0613 annotatedProperty IAO_0000115 @default.
- B13e2922594e62db2c8a5ab9f589a0613 annotatedSource MONDO_0018965 @default.
- B13e2922594e62db2c8a5ab9f589a0613 annotatedTarget "A genetic syndrome usually inherited as an X-link trait. It is caused by abnormalities in the COL4A5 gene. It affects males more often than females and is characterized by hematuria, progressive renal insufficiency, hearing loss, and ocular abnormalities." @default.