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- B1153f844a61c824c9ae30a21efa74cf8 hasDbXref "DOID:0060823" @default.
- B1153f844a61c824c9ae30a21efa74cf8 hasDbXref "PMID:17989220" @default.
- B1153f844a61c824c9ae30a21efa74cf8 hasDbXref "PMID:19449417" @default.
- B1153f844a61c824c9ae30a21efa74cf8 hasDbXref "PMID:24721225" @default.
- B1153f844a61c824c9ae30a21efa74cf8 type Axiom @default.
- B1153f844a61c824c9ae30a21efa74cf8 annotatedProperty IAO_0000115 @default.
- B1153f844a61c824c9ae30a21efa74cf8 annotatedSource MONDO_0010402 @default.
- B1153f844a61c824c9ae30a21efa74cf8 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.