Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B63b7cad4f6d02c4699cf0f47ccb2bf4d> ?p ?o ?g. }
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- B63b7cad4f6d02c4699cf0f47ccb2bf4d NCIT_P378 "ACC/AHA" @default.
- B63b7cad4f6d02c4699cf0f47ccb2bf4d type Axiom @default.
- B63b7cad4f6d02c4699cf0f47ccb2bf4d annotatedProperty NCIT_P325 @default.
- B63b7cad4f6d02c4699cf0f47ccb2bf4d annotatedSource NCIT_C43224 @default.
- B63b7cad4f6d02c4699cf0f47ccb2bf4d annotatedTarget "A chromosomal abnormality consisting of the presence of part or all of a third copy of chromosome 21 in somatic cells." @default.