Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B4d5e3a4397db9cc9003d2e48db660a5b> ?p ?o ?g. }
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- B4d5e3a4397db9cc9003d2e48db660a5b hasDbXref "NCIT:C84706" @default.
- B4d5e3a4397db9cc9003d2e48db660a5b type Axiom @default.
- B4d5e3a4397db9cc9003d2e48db660a5b annotatedProperty IAO_0000115 @default.
- B4d5e3a4397db9cc9003d2e48db660a5b annotatedSource MONDO_0009131 @default.
- B4d5e3a4397db9cc9003d2e48db660a5b annotatedTarget "A congenital disorder caused by mutations in the IKBKAP gene. It is characterized by damage of the sympathetic and parasympathetic and sensory nervous system." @default.