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- NCIT_C54583 IAO_0000115 "Terminology used in Individual Case Safety Reports for description of adverse event outcomes, section B2 of FDA MedWatch Form." @default.
- NCIT_C54583 NCIT_NHC0 "C54583" @default.
- NCIT_C54583 NCIT_P106 "Intellectual Product" @default.
- NCIT_C54583 NCIT_P108 "Adverse Event Outcome ICSR Terminology" @default.
- NCIT_C54583 NCIT_P207 "C1706740" @default.
- NCIT_C54583 NCIT_P322 "FDA" @default.
- NCIT_C54583 NCIT_P366 "Adverse_Event_Outcome_ICSR_Terminology" @default.
- NCIT_C54583 NCIT_P372 "Yes" @default.
- NCIT_C54583 NCIT_P376 "<p>Terminology used in individual case reports for voluntary and mandatory reporting of adverse reactions or adverse events during both pre and post approval periods of medical product development.</p><p> Terminology can be downloaded from this location: <a href="https://evs.nci.nih.gov/ftp1/FDA/ICSR">ICSR </a>.</p>" @default.
- NCIT_C54583 normalizedInformationContent "100" @default.
- NCIT_C54583 referenceCount "1" @default.
- NCIT_C54583 hasExactSynonym "Adverse Event Outcome ICSR Terminology" @default.
- NCIT_C54583 hasExactSynonym "Adverse Event Outcome Individual Case Safety Report Terminology" @default.
- NCIT_C54583 inSubset NCIT_C54447 @default.
- NCIT_C54583 type Class @default.
- NCIT_C54583 isDefinedBy ncit.owl @default.
- NCIT_C54583 label "Adverse Event Outcome ICSR Terminology" @default.
- NCIT_C54583 subClassOf NCIT_C131123 @default.
- NCIT_C54583 subClassOf NCIT_C16048 @default.
- NCIT_C54583 subClassOf NCIT_C20181 @default.
- NCIT_C54583 subClassOf NCIT_C20865 @default.
- NCIT_C54583 subClassOf NCIT_C54443 @default.
- NCIT_C54583 subClassOf NCIT_C54447 @default.
- NCIT_C54583 subClassOf NCIT_C54583 @default.