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- NCIT_C164681 NCIT_NHC0 "C164681" @default.
- NCIT_C164681 NCIT_P106 "Temporal Concept" @default.
- NCIT_C164681 NCIT_P108 "Adverse Event Occurrence Study Day Range" @default.
- NCIT_C164681 NCIT_P208 "CL977785" @default.
- NCIT_C164681 NCIT_P322 "BRIDG" @default.
- NCIT_C164681 NCIT_P325 "The relative timing for an adverse event expressed as the number of days offset from the study-defined reference activity (e.g., date of registration, start of treatment) for this particular experimental unit. EXAMPLE(S): Day 1, Days 10-20 OTHER NAME(S): NOTE(S): Derived from the occurrenceDateRange of this adverse event minus the dateRange of the reference activity + 1. The study-defined reference activity can be different from study to study. The study day for a date after this reference activity is a positive integer calculated as the difference in the two dates + 1. The study day for dates before the reference activity is a negative integer calculated as the difference between the two dates. Note that this means there is no "Day 0."" @default.
- NCIT_C164681 normalizedInformationContent "100" @default.
- NCIT_C164681 referenceCount "1" @default.
- NCIT_C164681 hasExactSynonym "Adverse Event Occurrence Study Day Range" @default.
- NCIT_C164681 hasExactSynonym "AdverseEvent.occurrenceStudyDayRange" @default.
- NCIT_C164681 inSubset NCIT_C159501 @default.
- NCIT_C164681 inSubset NCIT_C159504 @default.
- NCIT_C164681 type Class @default.
- NCIT_C164681 isDefinedBy ncit.owl @default.
- NCIT_C164681 label "Adverse Event Occurrence Study Day Range" @default.
- NCIT_C164681 subClassOf NCIT_C153132 @default.
- NCIT_C164681 subClassOf NCIT_C164681 @default.
- NCIT_C164681 subClassOf NCIT_C20181 @default.
- NCIT_C164681 subClassOf NCIT_C38013 @default.
- NCIT_C164681 subClassOf NCIT_C95349 @default.