Triple
T16605729
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | DK |
E403443
|
entity |
| Predicate | standsFor |
P590
|
FINISHED |
| Object | Diels–Kranz |
E1223397
|
NE FINISHED |
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: Diels–Kranz | Statement: [DK, standsFor, Diels–Kranz]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Diels–Kranz Context triple: [DK, standsFor, Diels–Kranz]
-
A.
Diels–Kranz
chosen
Diels–Kranz is the standard scholarly edition and numbering system for the surviving fragments and testimonia of the Presocratic philosophers.
-
B.
Diels–Alder reaction
The Diels–Alder reaction is a fundamental organic chemistry cycloaddition that forms six-membered rings by combining a conjugated diene with a dienophile in a single, stereospecific step.
-
C.
Eschenmoser–Claisen rearrangement
The Eschenmoser–Claisen rearrangement is a variant of the Claisen rearrangement in organic chemistry that converts allylic alcohols and amides into γ,δ-unsaturated carbonyl compounds via a [3,3]-sigmatropic rearrangement.
-
D.
Eschenmoser
Eschenmoser is a Swiss surname most notably associated with Albert Eschenmoser, a prominent organic chemist known for his pioneering work in the synthesis of complex natural products and studies on the origin of life.
-
E.
Chichibabin reaction
The Chichibabin reaction is an organic chemistry transformation that introduces an amino group into heteroaromatic compounds, especially pyridines, using sodium amide.
- F. None of above.
- G. Unsure - the case is ambiguous/there is not enough information to decide.
Provenance (3 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_69d883880d0c81908b5fcd454e767b60 |
completed | April 10, 2026, 4:58 a.m. |
| NER | Named-entity recognition | batch_69e36090cf388190b401c55230912104 |
completed | April 18, 2026, 10:44 a.m. |
| NED1 | Entity disambiguation (via context triple) | batch_6a007daa9f7c8190a9540d9a7a6ca6fb |
completed | May 10, 2026, 12:44 p.m. |
Created at: April 10, 2026, 5:17 a.m.