Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B22dbdd51e9f26680698c2fce3a0ab01f> ?p ?o ?g. }
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- B22dbdd51e9f26680698c2fce3a0ab01f hasDbXref "Orphanet:96264" @default.
- B22dbdd51e9f26680698c2fce3a0ab01f type Axiom @default.
- B22dbdd51e9f26680698c2fce3a0ab01f annotatedProperty IAO_0000115 @default.
- B22dbdd51e9f26680698c2fce3a0ab01f annotatedSource MONDO_0019929 @default.
- B22dbdd51e9f26680698c2fce3a0ab01f annotatedTarget "The 49,XXXXY syndrome represents a chromosomal anomaly of the aneuploidic type characterized by the presence of three extra X chromosomes in males." @default.