PropertyValue
?:definition
  • Documentation that describes an adverse event in clinical trial which is serious, as defined in the protocol. Reports may include but are not limited to specific regulatory forms and supporting data, reporter correspondence, associated note-to-files, source documentation, case logs, narratives, case unblinding forms, and/or safety database case printouts. [Adapted from TMF-RM]
?:hasCUIAnnotation
?:hasGeneratedBy
?:type

Metadata

Anon_0  
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<http://xmlns.com/foaf/0.1/primaryTopic> <https://research.tib.eu/covid-19/entity/C3897642_NCI_CareLex>
<http://xmlns.com/foaf/0.1/topic> Anon_0
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<http://purl.org/net/provenance/ns#createdBy>
Anon_1   (more)
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