Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B63cf92992ca342ed96a0e63f9c38b7c1> ?p ?o ?g. }
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- B63cf92992ca342ed96a0e63f9c38b7c1 NCIT_P378 "NCI" @default.
- B63cf92992ca342ed96a0e63f9c38b7c1 type Axiom @default.
- B63cf92992ca342ed96a0e63f9c38b7c1 annotatedProperty IAO_0000115 @default.
- B63cf92992ca342ed96a0e63f9c38b7c1 annotatedSource NCIT_C36630 @default.
- B63cf92992ca342ed96a0e63f9c38b7c1 annotatedTarget "A chromosomal abnormality consisting of the presence of one copy of the X chromosome and the complete absence of a second sex chromosome (X or Y) in somatic cells." @default.