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- Bc062c48aad5ae64c75d389453751d2f7 NCIT_P378 "CDISC-GLOSS" @default.
- Bc062c48aad5ae64c75d389453751d2f7 type Axiom @default.
- Bc062c48aad5ae64c75d389453751d2f7 annotatedProperty NCIT_P325 @default.
- Bc062c48aad5ae64c75d389453751d2f7 annotatedSource NCIT_C15601 @default.
- Bc062c48aad5ae64c75d389453751d2f7 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.