Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B5f257e47daf2fa11ea83dcc5ccfd2a39> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- B5f257e47daf2fa11ea83dcc5ccfd2a39 hasDbXref "Orphanet:96263" @default.
- B5f257e47daf2fa11ea83dcc5ccfd2a39 type Axiom @default.
- B5f257e47daf2fa11ea83dcc5ccfd2a39 annotatedProperty IAO_0000115 @default.
- B5f257e47daf2fa11ea83dcc5ccfd2a39 annotatedSource MONDO_0019928 @default.
- B5f257e47daf2fa11ea83dcc5ccfd2a39 annotatedTarget "The 48,XXXY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of two extra X chromosomes in males." @default.