Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Bba1e9d5c32c0853709d0d1bc4de36eb6> ?p ?o ?g. }
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- Bba1e9d5c32c0853709d0d1bc4de36eb6 hasDbXref "DOID:0060819" @default.
- Bba1e9d5c32c0853709d0d1bc4de36eb6 hasDbXref "PMID:10398239" @default.
- Bba1e9d5c32c0853709d0d1bc4de36eb6 type Axiom @default.
- Bba1e9d5c32c0853709d0d1bc4de36eb6 annotatedProperty IAO_0000115 @default.
- Bba1e9d5c32c0853709d0d1bc4de36eb6 annotatedSource MONDO_0010462 @default.
- Bba1e9d5c32c0853709d0d1bc4de36eb6 annotatedTarget "A syndromic X-linked intellectual disability characterized by moderate intellectual disability, seizures, dysmorphic facial features and in some older patients slowly progressive unsteady gait and progressive weakness that has material basis in variation in the chromosomal region Xq21.33-q23." @default.