Matches in Ubergraph for { <http://purl.obolibrary.org/obo/NCIT_C156629> ?p ?o ?g. }
Showing items 1 to 21 of
21
with 100 items per page.
- NCIT_C156629 IAO_0000115 "An adverse event that is reasonably expected and/or listed in the clinical protocol or other study-related document." @default.
- NCIT_C156629 NCIT_NHC0 "C156629" @default.
- NCIT_C156629 NCIT_P106 "Finding" @default.
- NCIT_C156629 NCIT_P108 "Anticipated Adverse Event" @default.
- NCIT_C156629 NCIT_P208 "CL935773" @default.
- NCIT_C156629 NCIT_P322 "CDISC-GLOSS" @default.
- NCIT_C156629 NCIT_P325 "Other adverse events that are not study endpoints and are not "expected" (i.e., because they are not in the investigator's brochure) that can be anticipated to occur with some frequency during the course of the trial, regardless of drug exposure, depending on the patient population and disease under study. NOTE: Examples of such "anticipated" events include known consequences of the underlying disease or condition under investigation, events anticipated from any background regimen, or re-emergence or worsening of a condition relative to pretreatment baseline. [after FDA, Guidance for Industry and Investigators: Safety Reporting Requirements for INDs and BA/BE Studies]" @default.
- NCIT_C156629 normalizedInformationContent "100" @default.
- NCIT_C156629 referenceCount "1" @default.
- NCIT_C156629 hasExactSynonym "Anticipated Adverse Event" @default.
- NCIT_C156629 hasExactSynonym "anticipated adverse event" @default.
- NCIT_C156629 inSubset NCIT_C61410 @default.
- NCIT_C156629 inSubset NCIT_C67497 @default.
- NCIT_C156629 type Class @default.
- NCIT_C156629 isDefinedBy ncit.owl @default.
- NCIT_C156629 label "Anticipated Adverse Event" @default.
- NCIT_C156629 subClassOf NCIT_C156629 @default.
- NCIT_C156629 subClassOf NCIT_C3367 @default.
- NCIT_C156629 subClassOf NCIT_C36291 @default.
- NCIT_C156629 subClassOf NCIT_C41331 @default.
- NCIT_C156629 subClassOf NCIT_C7057 @default.