Matches in Ubergraph for { <https://frink.apps.renci.org/.well-known/genid/Ba96a4fe2ee4d6e9f8acf9d6d494d8fb2> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- Ba96a4fe2ee4d6e9f8acf9d6d494d8fb2 NCIT_P378 "CDISC-GLOSS" @default.
- Ba96a4fe2ee4d6e9f8acf9d6d494d8fb2 type Axiom @default.
- Ba96a4fe2ee4d6e9f8acf9d6d494d8fb2 annotatedProperty NCIT_P325 @default.
- Ba96a4fe2ee4d6e9f8acf9d6d494d8fb2 annotatedSource NCIT_C16468 @default.
- Ba96a4fe2ee4d6e9f8acf9d6d494d8fb2 annotatedTarget "Document used during the informed consent process that is the basis for explaining, in understandable language, to potential subjects (or legally-authorized representative) the risks and potential benefits of a study and the rights and responsibilities of the parties involved. NOTE: The informed consent document provides a summary of a clinical trial (including its purpose, the treatment procedures and schedule, potential risks and benefits, alternatives to participation, etc.) and explains an individual's rights as a subject. [After FDA Informed Consent Information Sheet Guidance for IRBs, Clinical Investigators, and Sponsors, July 2014] See also informed consent." @default.