Triple
T22503947
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Medidata Solutions |
E556341
|
entity |
| Predicate | product |
P490
|
FINISHED |
| Object | Medidata Rave CTMS |
—
|
NE NERFINISHED |
How this triple was built (2 steps)
Every LLM step that produced this triple, in pipeline order — named-entity classification, the disambiguation choices (the exact options shown, with the pick highlighted), and the generated description. The batch + timestamp of each is in the Provenance table below.
NER
Named-entity recognition
gpt-5-mini
Instruction
Given a phrase, classify it is english named entity (e.g., persons, organizations, works of art) in Latin script, or not (e.g., literals, dates, URLs, verbose phrases). For disambiguation, the statement where the phrase occurs as object is also given. Please return a JSON object with `phrase` (string, the phrase being analyzed) and `is_ne` (boolean, indicating whether the phrase is a Named Entity).
Input
Phrase: Medidata Rave CTMS | Statement: [Medidata Solutions, product, Medidata Rave CTMS]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Medidata Rave CTMS Context triple: [Medidata Solutions, product, Medidata Rave CTMS]
-
A.
Clinical Trials Information System
The Clinical Trials Information System is the EU’s centralized online portal and database for the submission, assessment, authorization, and public transparency of clinical trials conducted in the European Union.
-
B.
Medidata Solutions
chosen
Medidata Solutions is a life sciences technology company best known for its cloud-based clinical trial and research platforms used by pharmaceutical, biotech, and medical device organizations.
-
C.
ICH E2A Clinical Safety Data Management
ICH E2A Clinical Safety Data Management is an international guideline that standardizes the collection, reporting, and evaluation of clinical safety data in drug development to support consistent pharmacovigilance and regulatory decision-making.
-
D.
eCTD
eCTD (electronic Common Technical Document) is a standardized, electronic format for submitting regulatory information on pharmaceuticals to health authorities worldwide.
-
E.
Regenstrief Medical Record System
The Regenstrief Medical Record System is an early, pioneering electronic medical record platform that helped shape modern health informatics and clinical data management practices.
- F. None of above.
- G. Unsure - the case is ambiguous/there is not enough information to decide.
Provenance (2 batches)
The batch behind each pipeline step, in order, with when it ran. Timestamps are batch-level — stages were processed in waves, so the object chain (NER → NED1 → NEDg → NED2) reads in order, but predicate / elicitation batches can sit in a different wave.
| Step | Stage | Batch ID | Status | When |
|---|---|---|---|---|
| creating | Elicitation | batch_69e11e555edc81909ca803587dafd747 |
completed | April 16, 2026, 5:37 p.m. |
| NER | Named-entity recognition | batch_69f15d5ac5808190a66f9111c350f4dc |
completed | April 29, 2026, 1:22 a.m. |
Created at: April 16, 2026, 8:50 p.m.