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- B2c74b3f191a2a4a6a2a1108945e0dd2e NCIT_P378 "CDISC-GLOSS" @default.
- B2c74b3f191a2a4a6a2a1108945e0dd2e type Axiom @default.
- B2c74b3f191a2a4a6a2a1108945e0dd2e annotatedProperty NCIT_P325 @default.
- B2c74b3f191a2a4a6a2a1108945e0dd2e annotatedSource NCIT_C40988 @default.
- B2c74b3f191a2a4a6a2a1108945e0dd2e annotatedTarget "A printed, optical, or electronic document designed to record all of the protocol-required information to be reported to the sponsor for each trial subject. NOTE: In common usage, CRF can refer to either a CRF page, which denotes a group of one or more data items, linked together for collection and display, or a casebook, which includes the entire group of CRF pages on which a set of clinical study observations can be or have been collected by completion of such CRF pages for a subject in a clinical study. See also CRF (paper), eCRF. [ICH E6 Glossary, FDA Final Guidance on eSource]." @default.