Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B8f44311a3212ae6e5f94b30567b89014> ?p ?o ?g. }
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- B8f44311a3212ae6e5f94b30567b89014 hasDbXref "Orphanet:10" @default.
- B8f44311a3212ae6e5f94b30567b89014 type Axiom @default.
- B8f44311a3212ae6e5f94b30567b89014 annotatedProperty IAO_0000115 @default.
- B8f44311a3212ae6e5f94b30567b89014 annotatedSource MONDO_0015028 @default.
- B8f44311a3212ae6e5f94b30567b89014 annotatedTarget "The 48,XXYY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of an extra X and Y chromosome in males." @default.