Triple

T22693379
Position Surface form Disambiguated ID Type / Status
Subject RNA polymerase II E561106 entity
Predicate hasPart P35 FINISHED
Object Rpb9 subunit NE NERFINISHED

How this triple was built (3 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: Rpb9 subunit | Statement: [RNA polymerase II, hasPart, Rpb9 subunit]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Rpb9 subunit
Context triple: [RNA polymerase II, hasPart, Rpb9 subunit]
  • A. Rpb7 subunit
    The Rpb7 subunit is a conserved protein component of eukaryotic RNA polymerase II that forms a subcomplex with Rpb4 and plays key roles in transcription initiation, elongation, and mRNA processing.
  • B. Pol II
    Pol II is the eukaryotic RNA polymerase enzyme complex responsible for transcribing protein-coding genes into messenger RNA.
  • C. fibrillarin
    Fibrillarin is a highly conserved nucleolar protein that functions as a core component of small nucleolar ribonucleoproteins (snoRNPs), playing a key role in rRNA processing and ribosome biogenesis.
  • D. RNA polymerase II
    RNA polymerase II is the eukaryotic enzyme complex responsible for transcribing DNA into messenger RNA and many non-coding RNAs, playing a central role in gene expression.
  • E. HCV NS5B RNA-dependent RNA polymerase
    HCV NS5B RNA-dependent RNA polymerase is the viral enzyme in hepatitis C virus responsible for replicating its RNA genome and a key target for direct-acting antiviral drugs.
  • F. None of above. chosen
  • G. Unsure - the case is ambiguous/there is not enough information to decide.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: Rpb9 subunit
Target entity description: The Rpb9 subunit is a small accessory component of eukaryotic RNA polymerase II that contributes to transcription fidelity and proper enzyme function.
  • A. Rpb7 subunit
    The Rpb7 subunit is a conserved protein component of eukaryotic RNA polymerase II that forms a subcomplex with Rpb4 and plays key roles in transcription initiation, elongation, and mRNA processing.
  • B. Pol II
    Pol II is the eukaryotic RNA polymerase enzyme complex responsible for transcribing protein-coding genes into messenger RNA.
  • C. fibrillarin
    Fibrillarin is a highly conserved nucleolar protein that functions as a core component of small nucleolar ribonucleoproteins (snoRNPs), playing a key role in rRNA processing and ribosome biogenesis.
  • D. RNA polymerase II
    RNA polymerase II is the eukaryotic enzyme complex responsible for transcribing DNA into messenger RNA and many non-coding RNAs, playing a central role in gene expression.
  • E. HCV NS5B RNA-dependent RNA polymerase
    HCV NS5B RNA-dependent RNA polymerase is the viral enzyme in hepatitis C virus responsible for replicating its RNA genome and a key target for direct-acting antiviral drugs.
  • F. None of above. chosen

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_69e2454d71b48190a1f80af9f82b6fcf completed April 17, 2026, 2:35 p.m.
NER Named-entity recognition batch_69f1789c6ae481908975b7d27e7624ac completed April 29, 2026, 3:18 a.m.
Created at: April 17, 2026, 3:13 p.m.