Triple

T19992809
Position Surface form Disambiguated ID Type / Status
Subject NMDA receptor E494104 entity
Predicate encodedBy P14248 FINISHED
Object GRIN2A
GRIN2A is a gene that encodes the GluN2A subunit of NMDA-type glutamate receptors, which are critical for synaptic plasticity, learning, and memory in the brain.
 E1407317 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: GRIN2A | Statement: [NMDA receptor, encodedBy, GRIN2A]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07 
Target entity: GRIN2A
Context triple: [NMDA receptor, encodedBy, GRIN2A]
  • A. GRIN1
    GRIN1 is a gene that encodes an essential subunit of NMDA-type glutamate receptors, which play a key role in synaptic transmission and plasticity in the central nervous system.
  • B. SCN1A
    SCN1A is a human gene encoding a neuronal voltage-gated sodium channel alpha subunit whose mutations are a major cause of Dravet syndrome and other epilepsy disorders.
  • C. GRIN2D
    GRIN2D is a gene that encodes the GluN2D subunit of NMDA-type glutamate receptors, which are critical for synaptic transmission and plasticity in the central nervous system.
  • D. GNAS
    GNAS is the abbreviation for the Georgian National Academy of Sciences, the leading scientific institution in Georgia that coordinates and promotes research across various disciplines.
  • E. HTT gene
    The HTT gene encodes the huntingtin protein, and mutations in this gene—particularly CAG trinucleotide repeat expansions—cause Huntington's disease, a progressive neurodegenerative disorder.
  • 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: GRIN2A
Triple: [NMDA receptor, encodedBy, GRIN2A]
Generated description
GRIN2A is a gene that encodes the GluN2A subunit of NMDA-type glutamate receptors, which are critical for synaptic plasticity, learning, and memory in the brain.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07 
Target entity: GRIN2A
Target entity description: GRIN2A is a gene that encodes the GluN2A subunit of NMDA-type glutamate receptors, which are critical for synaptic plasticity, learning, and memory in the brain.
  • A. GRIN1
    GRIN1 is a gene that encodes an essential subunit of NMDA-type glutamate receptors, which play a key role in synaptic transmission and plasticity in the central nervous system.
  • B. SCN1A
    SCN1A is a human gene encoding a neuronal voltage-gated sodium channel alpha subunit whose mutations are a major cause of Dravet syndrome and other epilepsy disorders.
  • C. GRIN2D
    GRIN2D is a gene that encodes the GluN2D subunit of NMDA-type glutamate receptors, which are critical for synaptic transmission and plasticity in the central nervous system.
  • D. GNAS
    GNAS is the abbreviation for the Georgian National Academy of Sciences, the leading scientific institution in Georgia that coordinates and promotes research across various disciplines.
  • E. HTT gene
    The HTT gene encodes the huntingtin protein, and mutations in this gene—particularly CAG trinucleotide repeat expansions—cause Huntington's disease, a progressive neurodegenerative disorder.
  • 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_69da626a67648190af9653832a3aeced completed April 11, 2026, 3:02 p.m.
NER Named-entity recognition batch_69e65fe2036c8190b9f313215ad44e87 completed April 20, 2026, 5:18 p.m.
NED1 Entity disambiguation (via context triple) batch_6a080e1c30c48190973e2735ecef8354 completed May 16, 2026, 6:26 a.m.
NEDg Description generation batch_6a08100875fc8190a60561870c8b6e32 completed May 16, 2026, 6:34 a.m.
NED2 Entity disambiguation (via description) batch_6a081080c9908190a6029049afe65004 completed May 16, 2026, 6:36 a.m.
Created at: April 11, 2026, 3:31 p.m.