Triple
T1759109
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | Campylobacter |
E38614
|
entity |
| Predicate | complication |
P18423
|
FINISHED |
| Object |
Guillain–Barré syndrome
Guillain–Barré syndrome is an acute autoimmune disorder in which the immune system attacks peripheral nerves, leading to rapidly progressive muscle weakness and potential paralysis, often triggered by infections such as Campylobacter.
|
E196711
|
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: Guillain–Barré syndrome | Statement: [Campylobacter, complication, Guillain–Barré syndrome]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: Guillain–Barré syndrome Context triple: [Campylobacter, complication, Guillain–Barré syndrome]
-
A.
spinal muscular atrophy
Spinal muscular atrophy is a genetic neuromuscular disorder characterized by progressive muscle weakness and atrophy due to degeneration of motor neurons in the spinal cord.
-
B.
ALS
ALS (amyotrophic lateral sclerosis) is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord, leading to muscle weakness, paralysis, and ultimately respiratory failure.
-
C.
relapsing-remitting multiple sclerosis
Relapsing-remitting multiple sclerosis is the most common form of multiple sclerosis, characterized by clearly defined attacks of neurological symptoms followed by periods of partial or complete recovery.
-
D.
progressive multifocal leukoencephalopathy
Progressive multifocal leukoencephalopathy is a rare, often fatal demyelinating brain disease caused by reactivation of the JC virus in immunocompromised individuals, leading to rapidly progressive neurological decline.
-
E.
Leigh-Mallory
Leigh-Mallory is the surname of a prominent British military family, most notably borne by Air Chief Marshal Trafford Leigh-Mallory, a senior Royal Air Force commander during the Second World War.
- 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: Guillain–Barré syndrome Triple: [Campylobacter, complication, Guillain–Barré syndrome]
Generated description
Guillain–Barré syndrome is an acute autoimmune disorder in which the immune system attacks peripheral nerves, leading to rapidly progressive muscle weakness and potential paralysis, often triggered by infections such as Campylobacter.
NED2
Entity disambiguation (via description)
gpt-5-mini-2025-08-07
Target entity: Guillain–Barré syndrome Target entity description: Guillain–Barré syndrome is an acute autoimmune disorder in which the immune system attacks peripheral nerves, leading to rapidly progressive muscle weakness and potential paralysis, often triggered by infections such as Campylobacter.
-
A.
spinal muscular atrophy
Spinal muscular atrophy is a genetic neuromuscular disorder characterized by progressive muscle weakness and atrophy due to degeneration of motor neurons in the spinal cord.
-
B.
ALS
ALS (amyotrophic lateral sclerosis) is a progressive neurodegenerative disease that affects nerve cells in the brain and spinal cord, leading to muscle weakness, paralysis, and ultimately respiratory failure.
-
C.
relapsing-remitting multiple sclerosis
Relapsing-remitting multiple sclerosis is the most common form of multiple sclerosis, characterized by clearly defined attacks of neurological symptoms followed by periods of partial or complete recovery.
-
D.
progressive multifocal leukoencephalopathy
Progressive multifocal leukoencephalopathy is a rare, often fatal demyelinating brain disease caused by reactivation of the JC virus in immunocompromised individuals, leading to rapidly progressive neurological decline.
-
E.
Leigh-Mallory
Leigh-Mallory is the surname of a prominent British military family, most notably borne by Air Chief Marshal Trafford Leigh-Mallory, a senior Royal Air Force commander during the Second World War.
- 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_69a8862d562481908d7025a1c1f67c0d |
completed | March 4, 2026, 7:21 p.m. |
| NER | Named-entity recognition | batch_69aa643f6a188190a250d5982badcce5 |
completed | March 6, 2026, 5:21 a.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69ada0ec80f48190bcdc92e5ed4e44e6 |
completed | March 8, 2026, 4:16 p.m. |
| NEDg | Description generation | batch_69ada1e3587c8190bca329c68ff31c41 |
completed | March 8, 2026, 4:20 p.m. |
| NED2 | Entity disambiguation (via description) | batch_69ada2977bfc8190ad028e17184fccaa |
completed | March 8, 2026, 4:23 p.m. |
Created at: March 4, 2026, 7:31 p.m.