Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/B7fcf6f9a708a2a5b76c6e622b031ff58> ?p ?o ?g. }
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- B7fcf6f9a708a2a5b76c6e622b031ff58 NCIT_P378 "NCI" @default.
- B7fcf6f9a708a2a5b76c6e622b031ff58 type Axiom @default.
- B7fcf6f9a708a2a5b76c6e622b031ff58 annotatedProperty IAO_0000115 @default.
- B7fcf6f9a708a2a5b76c6e622b031ff58 annotatedSource NCIT_C96814 @default.
- B7fcf6f9a708a2a5b76c6e622b031ff58 annotatedTarget "A role used to assert a relationship between a disease, disorder or finding and a chromosome. This restriction should be used when a disease or disorder maps to a chromosome. It is not meant to be used when a specific cytogenetic abnormality is known (e.g. translocation, inversion). The domain and range for this role are 'Disease, Disorder or Finding' and 'Chromosome', respectively. The range for this role excludes chromosomal bands and physical locations." @default.