Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B665a6c91c881a9d8bc318311f2ff93bf> ?p ?o ?g. }
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- B665a6c91c881a9d8bc318311f2ff93bf hasDbXref "EFO:0004128" @default.
- B665a6c91c881a9d8bc318311f2ff93bf type Axiom @default.
- B665a6c91c881a9d8bc318311f2ff93bf annotatedProperty IAO_0000115 @default.
- B665a6c91c881a9d8bc318311f2ff93bf annotatedSource MONDO_0005334 @default.
- B665a6c91c881a9d8bc318311f2ff93bf annotatedTarget "A group of inherited conditions characterized initially by hematuria and slowly progressing to renal insufficiency. The most common form is the Alport syndrome (hereditary nephritis with hearing loss) which is caused by mutations in genes for type IV collagen and defective glomerular basement membrane." @default.