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- B8c3614f2ee44a96f3c0ae2a4dc55977a hasDbXref "DOID:0060823" @default.
- B8c3614f2ee44a96f3c0ae2a4dc55977a hasDbXref "PMID:17989220" @default.
- B8c3614f2ee44a96f3c0ae2a4dc55977a hasDbXref "PMID:19449417" @default.
- B8c3614f2ee44a96f3c0ae2a4dc55977a hasDbXref "PMID:24721225" @default.
- B8c3614f2ee44a96f3c0ae2a4dc55977a type Axiom @default.
- B8c3614f2ee44a96f3c0ae2a4dc55977a annotatedProperty IAO_0000115 @default.
- B8c3614f2ee44a96f3c0ae2a4dc55977a annotatedSource MONDO_0010402 @default.
- B8c3614f2ee44a96f3c0ae2a4dc55977a annotatedTarget "A syndromic X-linked intellectual disability characterized by moderate intellectual disability with variable occurrence of asthenic body habitus, dysmorphic features, autistic features, macrocephaly, seizures, myoclonic jerks, and hyporeflexia that has material basis in mutation in the GRIA3 gene on chromosome Xq25." @default.