Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B3ef49b228d582ae7d40b057648cede40> ?p ?o ?g. }
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- B3ef49b228d582ae7d40b057648cede40 hasDbXref "NCIT:C34842" @default.
- B3ef49b228d582ae7d40b057648cede40 type Axiom @default.
- B3ef49b228d582ae7d40b057648cede40 annotatedProperty IAO_0000115 @default.
- B3ef49b228d582ae7d40b057648cede40 annotatedSource MONDO_0018965 @default.
- B3ef49b228d582ae7d40b057648cede40 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.