Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Ba567b0fbb01a8f413682d93dd37c8273> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Ba567b0fbb01a8f413682d93dd37c8273 hasDbXref "Orphanet:718" @default.
- Ba567b0fbb01a8f413682d93dd37c8273 type Axiom @default.
- Ba567b0fbb01a8f413682d93dd37c8273 annotatedProperty IAO_0000115 @default.
- Ba567b0fbb01a8f413682d93dd37c8273 annotatedSource MONDO_0009869 @default.
- Ba567b0fbb01a8f413682d93dd37c8273 annotatedTarget "Pierre-Robin syndrome (or Pierre-Robin sequence) is characterized by triad of orofacial morphological anomalies consisting of retrognathism, glossoptosis and a posterior median velopalatal cleft." @default.