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- Bf0e9d28e4a86b0925e3d54e26f596480 hasDbXref "DOID:0110951" @default.
- Bf0e9d28e4a86b0925e3d54e26f596480 hasDbXref "PMID:11810298" @default.
- Bf0e9d28e4a86b0925e3d54e26f596480 hasDbXref "PMID:20127975" @default.
- Bf0e9d28e4a86b0925e3d54e26f596480 type Axiom @default.
- Bf0e9d28e4a86b0925e3d54e26f596480 annotatedProperty IAO_0000115 @default.
- Bf0e9d28e4a86b0925e3d54e26f596480 annotatedSource MONDO_0011697 @default.
- Bf0e9d28e4a86b0925e3d54e26f596480 annotatedTarget "A Waardenburg's syndrome characterized by pigmentary abnormalities of the hair, skin, and eyes, congenital sensorineural hearing loss, and absence of lateral displacement of the inner canthus of each eye that has material basis in variation in the chromosome region 8p23." @default.