Triple

T5873304

Position	Surface form	Disambiguated ID	Type / Status
Subject	Paediatric Regulation	`E130568`	entity
Predicate	officialName	`P66`	FINISHED
Object	Regulation (EC) No 1901/2006 Regulation (EC) No 1901/2006 is the European Union’s Paediatric Regulation, establishing rules to ensure that medicines for children are researched, developed, and authorized to the same high standards as those for adults.	`E563353`	NE FINISHED

How this triple was built (4 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: Regulation (EC) No 1901/2006 | Statement: [Paediatric Regulation, officialName, Regulation (EC) No 1901/2006]

NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07

Target entity: Regulation (EC) No 1901/2006
Context triple: [Paediatric Regulation, officialName, Regulation (EC) No 1901/2006]

A. Regulation (EC) No 726/2004
Regulation (EC) No 726/2004 is an EU law that establishes the centralized procedure for the authorization and supervision of medicinal products and defines the role and powers of the European Medicines Agency.
B. Regulation (EC) No 294/2008
Regulation (EC) No 294/2008 is the EU legislative act that established the European Institute of Innovation and Technology and set out its mission, structure, and operating framework.
C. Regulation (EC) No 851/2004
Regulation (EC) No 851/2004 is the EU law that established the European Centre for Disease Prevention and Control and defined its mandate, structure, and functions in coordinating infectious disease surveillance and control across member states.
D. Regulation (EC) No 141/2000
Regulation (EC) No 141/2000 is the European Union’s core legal framework establishing incentives and procedures for the designation, development, and authorization of orphan medicinal products for rare diseases.
E. Regulation (EC) No 45/2001
Regulation (EC) No 45/2001 is an EU law that sets out data protection rules for the processing of personal data by EU institutions and bodies.
F. None of above. chosen
G. Unsure - the case is ambiguous/there is not enough information to decide.

NEDg Description generation gpt-5.1

Instruction

Generate a one-sentence description of the target entity. 
You are given a context triple in the form (subject, predicate, object), where the object is the target entity. 
# Instructions
Use the triple to infer relevant information about the entity. Describe the entity based on what is most defining, well-known. 
Avoid repeating the information from the triple, unless really essential.
# Response Format
Return only the sentence: "Description: [one-sentence description of the target entity]"

Input

Entity: Regulation (EC) No 1901/2006
Triple: [Paediatric Regulation, officialName, Regulation (EC) No 1901/2006]

Generated description

Regulation (EC) No 1901/2006 is the European Union’s Paediatric Regulation, establishing rules to ensure that medicines for children are researched, developed, and authorized to the same high standards as those for adults.

NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07

Target entity: Regulation (EC) No 1901/2006
Target entity description: Regulation (EC) No 1901/2006 is the European Union’s Paediatric Regulation, establishing rules to ensure that medicines for children are researched, developed, and authorized to the same high standards as those for adults.

A. Regulation (EC) No 726/2004
Regulation (EC) No 726/2004 is an EU law that establishes the centralized procedure for the authorization and supervision of medicinal products and defines the role and powers of the European Medicines Agency.
B. Regulation (EC) No 294/2008
Regulation (EC) No 294/2008 is the EU legislative act that established the European Institute of Innovation and Technology and set out its mission, structure, and operating framework.
C. Regulation (EC) No 851/2004
Regulation (EC) No 851/2004 is the EU law that established the European Centre for Disease Prevention and Control and defined its mandate, structure, and functions in coordinating infectious disease surveillance and control across member states.
D. Regulation (EC) No 141/2000
Regulation (EC) No 141/2000 is the European Union’s core legal framework establishing incentives and procedures for the designation, development, and authorization of orphan medicinal products for rare diseases.
E. Regulation (EC) No 45/2001
Regulation (EC) No 45/2001 is an EU law that sets out data protection rules for the processing of personal data by EU institutions and bodies.
F. None of above. chosen

Provenance (5 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_69c0085047dc8190af24e311edad3c07`	completed	March 22, 2026, 3:18 p.m.
NER	Named-entity recognition	`batch_69c035f99b788190b5b06d83b9499bfa`	completed	March 22, 2026, 6:33 p.m.
NED1	Entity disambiguation (via context triple)	`batch_69c1134931c48190b4a849c8f16723e3`	completed	March 23, 2026, 10:17 a.m.
NEDg	Description generation	`batch_69c113de5d788190affa46cf416d180d`	completed	March 23, 2026, 10:20 a.m.
NED2	Entity disambiguation (via description)	`batch_69c1144e77f881908ab59a67160c1630`	completed	March 23, 2026, 10:22 a.m.

Created at: March 22, 2026, 3:57 p.m.