Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Be896a89f1fb668821a49538f7794a61c> ?p ?o ?g. }
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- Be896a89f1fb668821a49538f7794a61c hasDbXref "MONDO:Lexical" @default.
- Be896a89f1fb668821a49538f7794a61c hasDbXref "OMIM:616326" @default.
- Be896a89f1fb668821a49538f7794a61c type Axiom @default.
- Be896a89f1fb668821a49538f7794a61c annotatedProperty hasRelatedSynonym @default.
- Be896a89f1fb668821a49538f7794a61c annotatedSource MONDO_0014588 @default.
- Be896a89f1fb668821a49538f7794a61c annotatedTarget "myasthenic syndrome, congenital, 11, associated with acetylcholine receptor deficiency" @default.