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.