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- Bace0eb51e30b1f613672fc7e502fea4a NCIT_P378 "CDISC-GLOSS" @default.
- Bace0eb51e30b1f613672fc7e502fea4a type Axiom @default.
- Bace0eb51e30b1f613672fc7e502fea4a annotatedProperty NCIT_P325 @default.
- Bace0eb51e30b1f613672fc7e502fea4a annotatedSource NCIT_C15601 @default.
- Bace0eb51e30b1f613672fc7e502fea4a annotatedTarget "Phase that includes the controlled clinical trials conducted to evaluate the safety and efficacy of the drug in a limited number of patients with the disease or condition under study. Objectives can be dose-ranging (dose-response, frequency of dosing), type of patients, or numerous other characteristics of safety and efficacy. [After 21 CRF Part 312.21 Phases of an investigation] See also phase, phase 2a, phase 2b." @default.