Triple

T16605686
Position Surface form Disambiguated ID Type / Status
Subject Die Fragmente der Vorsokratiker E403442 entity
Predicate alsoKnownAs P39 FINISHED
Object Diels–Kranz
Diels–Kranz is the standard scholarly edition and numbering system for the surviving fragments and testimonia of the Presocratic philosophers.
E1223397 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: Diels–Kranz | Statement: [Die Fragmente der Vorsokratiker, alsoKnownAs, Diels–Kranz]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Diels–Kranz
Context triple: [Die Fragmente der Vorsokratiker, alsoKnownAs, Diels–Kranz]
  • A. 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.
  • B. 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.
  • C. 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.
  • D. Chichibabin reaction
    The Chichibabin reaction is an organic chemistry transformation that introduces an amino group into heteroaromatic compounds, especially pyridines, using sodium amide.
  • E. Claisen rearrangement
    The Claisen rearrangement is a pericyclic [3,3]-sigmatropic rearrangement in organic chemistry that converts allyl vinyl ethers (or related systems) into γ,δ-unsaturated carbonyl compounds with high stereospecificity.
  • 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: Diels–Kranz
Triple: [Die Fragmente der Vorsokratiker, alsoKnownAs, Diels–Kranz]
Generated description
Diels–Kranz is the standard scholarly edition and numbering system for the surviving fragments and testimonia of the Presocratic philosophers.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: Diels–Kranz
Target entity description: Diels–Kranz is the standard scholarly edition and numbering system for the surviving fragments and testimonia of the Presocratic philosophers.
  • A. 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.
  • B. 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.
  • C. 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.
  • D. Chichibabin reaction
    The Chichibabin reaction is an organic chemistry transformation that introduces an amino group into heteroaromatic compounds, especially pyridines, using sodium amide.
  • E. Claisen rearrangement
    The Claisen rearrangement is a pericyclic [3,3]-sigmatropic rearrangement in organic chemistry that converts allyl vinyl ethers (or related systems) into γ,δ-unsaturated carbonyl compounds with high stereospecificity.
  • 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_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_6a0075a8a6248190a9e2bb469d821c66 completed May 10, 2026, 12:10 p.m.
NEDg Description generation batch_6a007705f57881908b07a20ae8957c64 completed May 10, 2026, 12:16 p.m.
NED2 Entity disambiguation (via description) batch_6a007b18f0b08190a9ddc6ad7358d6b8 completed May 10, 2026, 12:33 p.m.
Created at: April 10, 2026, 5:17 a.m.