Triple
T22457932
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Common Technical Document |
E555160
|
entity |
| Predicate | relatedTo |
P37
|
FINISHED |
| Object | eCTD |
—
|
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: eCTD | Statement: [Common Technical Document, relatedTo, eCTD]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: eCTD Context triple: [Common Technical Document, relatedTo, eCTD]
-
A.
eCTD
chosen
eCTD (electronic Common Technical Document) is a standardized, electronic format for submitting regulatory information on pharmaceuticals to health authorities worldwide.
-
B.
eCTD is the electronic implementation of the CTD format
eCTD is a standardized electronic format used for submitting regulatory information, such as drug approval applications, to health authorities.
-
C.
International Council for Harmonisation guideline E2C
International Council for Harmonisation guideline E2C is a regulatory framework that provides standardized requirements for the ongoing safety evaluation and periodic benefit-risk assessment of marketed medicinal products.
-
D.
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.
-
E.
ICH E6 Good Clinical Practice
ICH E6 Good Clinical Practice is an international ethical and scientific quality standard that governs the design, conduct, recording, and reporting of clinical trials involving human subjects.
- 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_69e11e51fdec8190adfdf9f8a6362221 |
completed | April 16, 2026, 5:37 p.m. |
| NER | Named-entity recognition | batch_69f15b7d00208190955a70e2c22d25a4 |
completed | April 29, 2026, 1:14 a.m. |
Created at: April 16, 2026, 8:48 p.m.