Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B0a2ded0c12dbc26d469e0dbe6a59d10c> ?p ?o ?g. }
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- B0a2ded0c12dbc26d469e0dbe6a59d10c hasDbXref "Orphanet:238446" @default.
- B0a2ded0c12dbc26d469e0dbe6a59d10c type Axiom @default.
- B0a2ded0c12dbc26d469e0dbe6a59d10c annotatedProperty IAO_0000115 @default.
- B0a2ded0c12dbc26d469e0dbe6a59d10c annotatedSource MONDO_0012081 @default.
- B0a2ded0c12dbc26d469e0dbe6a59d10c annotatedTarget "The 15q11-q13 microduplication (dup15q11-q13) syndrome is characterized by neurobehavioral disorders, hypotonia, cognitive deficit, language delay and seizures. Prevalence is unknown." @default.