Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B7d8ba7af9ebcc15e8a59b396dc8230b3> ?p ?o ?g. }
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- B7d8ba7af9ebcc15e8a59b396dc8230b3 hasDbXref "DOID:0110951" @default.
- B7d8ba7af9ebcc15e8a59b396dc8230b3 hasDbXref "PMID:11810298" @default.
- B7d8ba7af9ebcc15e8a59b396dc8230b3 hasDbXref "PMID:20127975" @default.
- B7d8ba7af9ebcc15e8a59b396dc8230b3 type Axiom @default.
- B7d8ba7af9ebcc15e8a59b396dc8230b3 annotatedProperty IAO_0000115 @default.
- B7d8ba7af9ebcc15e8a59b396dc8230b3 annotatedSource MONDO_0011697 @default.
- B7d8ba7af9ebcc15e8a59b396dc8230b3 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.