Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B8c8b607f6f1decd5cf8b4cfb091c13b5> ?p ?o ?g. }
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- B8c8b607f6f1decd5cf8b4cfb091c13b5 hasDbXref "MONDO:patterns/disease_series_by_gene" @default.
- B8c8b607f6f1decd5cf8b4cfb091c13b5 type Axiom @default.
- B8c8b607f6f1decd5cf8b4cfb091c13b5 annotatedProperty IAO_0000115 @default.
- B8c8b607f6f1decd5cf8b4cfb091c13b5 annotatedSource MONDO_0014482 @default.
- B8c8b607f6f1decd5cf8b4cfb091c13b5 annotatedTarget "Any intellectual disability-expressive aphasia-facial dysmorphism syndrome in which the cause of the disease is a mutation in the SETBP1 gene." @default.