Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B8bf526029bffd1b6fb6742ee77ff9312> ?p ?o ?g. }
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- B8bf526029bffd1b6fb6742ee77ff9312 hasDbXref "Orphanet:171829" @default.
- B8bf526029bffd1b6fb6742ee77ff9312 type Axiom @default.
- B8bf526029bffd1b6fb6742ee77ff9312 annotatedProperty IAO_0000115 @default.
- B8bf526029bffd1b6fb6742ee77ff9312 annotatedSource MONDO_0015749 @default.
- B8bf526029bffd1b6fb6742ee77ff9312 annotatedTarget "Deletion 6q16 syndrome is a Prader-Willi like syndrome characterized by obesity, hyperphagia, hypotonia, small hands and feet, eye/vision anomalies, and global developmental delay." @default.