Triple

T15360828
Position Surface form Disambiguated ID Type / Status
Subject A Crack in Creation: Gene Editing and the Unthinkable Power to Control Evolution E367283 entity
Predicate mainSubject P3 FINISHED
Object CRISPR E366097 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: CRISPR | Statement: [A Crack in Creation: Gene Editing and the Unthinkable Power to Control Evolution, mainSubject, CRISPR]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: CRISPR
Context triple: [A Crack in Creation: Gene Editing and the Unthinkable Power to Control Evolution, mainSubject, CRISPR]
  • A. CRISPR-Cas9 gene-editing technology chosen
    CRISPR-Cas9 gene-editing technology is a revolutionary molecular tool that allows scientists to precisely modify DNA within living organisms, transforming research, medicine, and biotechnology.
  • B. Cpf1 (Cas12a)
    Cpf1 (Cas12a) is a CRISPR-associated endonuclease used for genome editing that recognizes different DNA target sequences and creates staggered cuts, offering distinct advantages and applications compared to Cas9.
  • C. SaCas9
    SaCas9 is a compact Cas9 nuclease derived from Staphylococcus aureus that enables CRISPR-based genome editing, particularly useful where smaller delivery vectors such as AAV are required.
  • D. A Crack in Creation: Gene Editing and the Unthinkable Power to Control Evolution
    "A Crack in Creation: Gene Editing and the Unthinkable Power to Control Evolution" is a popular science book that explains the discovery, science, and ethical implications of CRISPR gene-editing technology for reshaping life and evolution.
  • E. Yamanaka factors
    Yamanaka factors are a set of transcription factors that can reprogram adult somatic cells into induced pluripotent stem cells, revolutionizing regenerative medicine and stem cell research.
  • 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_69d85a1483788190ad93c2748e8af34b completed April 10, 2026, 2:01 a.m.
NER Named-entity recognition batch_69e03e4607408190ab281a7f7a8012d3 completed April 16, 2026, 1:41 a.m.
NED1 Entity disambiguation (via context triple) batch_69ff0b4a181c8190bffc1ac1a86e215d completed May 9, 2026, 10:24 a.m.
Created at: April 10, 2026, 3:18 a.m.