Triple

T13255994
Position Surface form Disambiguated ID Type / Status
Subject James Padraig Farrell E315658 entity
Predicate hasMedicalCondition P1005 FINISHED
Object Angelman syndrome
Angelman syndrome is a rare genetic neurodevelopmental disorder characterized by severe intellectual disability, speech impairment, movement and balance problems, and a typically happy, excitable demeanor.
E1030536 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: Angelman syndrome | Statement: [James Padraig Farrell, hasMedicalCondition, Angelman syndrome]
NED1 Entity disambiguation (via context triple) gpt-5-mini-2025-08-07
Target entity: Angelman syndrome
Context triple: [James Padraig Farrell, hasMedicalCondition, Angelman syndrome]
  • A. Dravet syndrome
    Dravet syndrome is a rare, severe form of early-onset epilepsy characterized by prolonged, drug-resistant seizures and developmental delays, typically beginning in infancy.
  • B. Lennox-Gastaut syndrome
    Lennox-Gastaut syndrome is a severe, childhood-onset epileptic encephalopathy characterized by multiple types of drug-resistant seizures, cognitive impairment, and abnormal EEG findings.
  • C. Krabbe disease
    Krabbe disease is a rare, inherited neurodegenerative disorder that destroys the protective myelin sheath of nerve cells in the brain and nervous system, typically leading to severe developmental regression and early death in infancy or childhood.
  • D. MPS II
    MPS II, also known as Hunter syndrome, is a rare X-linked lysosomal storage disorder caused by iduronate-2-sulfatase deficiency, leading to progressive multi-organ dysfunction and developmental impairment.
  • E. tuberous sclerosis complex
    Tuberous sclerosis complex is a genetic disorder characterized by benign tumors in multiple organs, often leading to epilepsy, developmental delays, and skin abnormalities.
  • 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: Angelman syndrome
Triple: [James Padraig Farrell, hasMedicalCondition, Angelman syndrome]
Generated description
Angelman syndrome is a rare genetic neurodevelopmental disorder characterized by severe intellectual disability, speech impairment, movement and balance problems, and a typically happy, excitable demeanor.
NED2 Entity disambiguation (via description) gpt-5-mini-2025-08-07
Target entity: Angelman syndrome
Target entity description: Angelman syndrome is a rare genetic neurodevelopmental disorder characterized by severe intellectual disability, speech impairment, movement and balance problems, and a typically happy, excitable demeanor.
  • A. Dravet syndrome
    Dravet syndrome is a rare, severe form of early-onset epilepsy characterized by prolonged, drug-resistant seizures and developmental delays, typically beginning in infancy.
  • B. Lennox-Gastaut syndrome
    Lennox-Gastaut syndrome is a severe, childhood-onset epileptic encephalopathy characterized by multiple types of drug-resistant seizures, cognitive impairment, and abnormal EEG findings.
  • C. Krabbe disease
    Krabbe disease is a rare, inherited neurodegenerative disorder that destroys the protective myelin sheath of nerve cells in the brain and nervous system, typically leading to severe developmental regression and early death in infancy or childhood.
  • D. MPS II
    MPS II, also known as Hunter syndrome, is a rare X-linked lysosomal storage disorder caused by iduronate-2-sulfatase deficiency, leading to progressive multi-organ dysfunction and developmental impairment.
  • E. tuberous sclerosis complex
    Tuberous sclerosis complex is a genetic disorder characterized by benign tumors in multiple organs, often leading to epilepsy, developmental delays, and skin abnormalities.
  • 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_69d806b1d9ac8190852c5571d5bd5f0f completed April 9, 2026, 8:06 p.m.
NER Named-entity recognition batch_69d98f7614fc8190a1cac076d706e9aa completed April 11, 2026, 12:01 a.m.
NED1 Entity disambiguation (via context triple) batch_69f70a4240d881909f0ee898fd272826 completed May 3, 2026, 8:41 a.m.
NEDg Description generation batch_69f70c9718d08190b09fc6723712ef55 completed May 3, 2026, 8:51 a.m.
NED2 Entity disambiguation (via description) batch_69f70d32b38881909d500b81a0164bda completed May 3, 2026, 8:54 a.m.
Created at: April 9, 2026, 9:24 p.m.