Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B34e1e8e8c966a6b2cb936afcea05ff16> ?p ?o ?g. }
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- B34e1e8e8c966a6b2cb936afcea05ff16 hasDbXref "NCIT:C124510" @default.
- B34e1e8e8c966a6b2cb936afcea05ff16 type Axiom @default.
- B34e1e8e8c966a6b2cb936afcea05ff16 annotatedProperty IAO_0000115 @default.
- B34e1e8e8c966a6b2cb936afcea05ff16 annotatedSource MONDO_0015411 @default.
- B34e1e8e8c966a6b2cb936afcea05ff16 annotatedTarget "A congenital abnormality consisting of an opening or gap in the face, which results from incomplete fusion of one or more of the embryonic facial prominences." @default.