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- Be5764cb17e1a33fc4fbd6b50b58d5f5f NCIT_P378 "NCI" @default.
- Be5764cb17e1a33fc4fbd6b50b58d5f5f type Axiom @default.
- Be5764cb17e1a33fc4fbd6b50b58d5f5f annotatedProperty IAO_0000115 @default.
- Be5764cb17e1a33fc4fbd6b50b58d5f5f annotatedSource NCIT_R174 @default.
- Be5764cb17e1a33fc4fbd6b50b58d5f5f 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.