Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B701f0c466ce10c4dae804ccaf223882d> ?p ?o ?g. }
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- B701f0c466ce10c4dae804ccaf223882d hasDbXref "NCIT:C36410" @default.
- B701f0c466ce10c4dae804ccaf223882d type Axiom @default.
- B701f0c466ce10c4dae804ccaf223882d annotatedProperty IAO_0000115 @default.
- B701f0c466ce10c4dae804ccaf223882d annotatedSource MONDO_0022174 @default.
- B701f0c466ce10c4dae804ccaf223882d annotatedTarget "A cytogenetic abnormality that refers to the allelic loss of all or part of the short arm of chromosome 12." @default.