Triple
T11074432
| Position | Surface form | Disambiguated ID | Type / Status |
|---|---|---|---|
| Subject | CD20 protein |
E261827
|
entity |
| Predicate | therapeuticArea |
P20980
|
FINISHED |
| Object |
microscopic polyangiitis
Microscopic polyangiitis is a rare autoimmune small-vessel vasculitis that causes inflammation and damage in organs such as the kidneys, lungs, and nerves, often associated with anti-neutrophil cytoplasmic antibodies (ANCA).
|
E902884
|
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: microscopic polyangiitis | Statement: [CD20 protein, therapeuticArea, microscopic polyangiitis]
NED1
Entity disambiguation (via context triple)
gpt-5-mini-2025-08-07
Target entity: microscopic polyangiitis Context triple: [CD20 protein, therapeuticArea, microscopic polyangiitis]
-
A.
Wegener's granulomatosis
Wegener's granulomatosis, now more commonly called granulomatosis with polyangiitis, is a rare autoimmune disease characterized by inflammation of blood vessels that can damage organs such as the lungs, kidneys, and upper respiratory tract.
-
B.
PR3-ANCA
PR3-ANCA is an autoantibody directed against proteinase 3 that is strongly associated with granulomatosis with polyangiitis (formerly Wegener's granulomatosis) and used as a key diagnostic marker for this vasculitic disease.
-
C.
Behçet's disease
Behçet's disease is a rare, chronic inflammatory disorder characterized by recurrent mouth and genital ulcers, eye inflammation, and systemic vasculitis affecting multiple organ systems.
-
D.
erythema nodosum
Erythema nodosum is an inflammatory condition characterized by tender red nodules, usually on the shins, often associated with systemic diseases such as infections, autoimmune disorders, and inflammatory bowel disease.
-
E.
Behçet
Behçet is a Turkish surname most notably associated with dermatologist Hulusi Behçet, after whom Behçet's disease is named.
- 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: microscopic polyangiitis Triple: [CD20 protein, therapeuticArea, microscopic polyangiitis]
Generated description
Microscopic polyangiitis is a rare autoimmune small-vessel vasculitis that causes inflammation and damage in organs such as the kidneys, lungs, and nerves, often associated with anti-neutrophil cytoplasmic antibodies (ANCA).
NED2
Entity disambiguation (via description)
gpt-5-mini-2025-08-07
Target entity: microscopic polyangiitis Target entity description: Microscopic polyangiitis is a rare autoimmune small-vessel vasculitis that causes inflammation and damage in organs such as the kidneys, lungs, and nerves, often associated with anti-neutrophil cytoplasmic antibodies (ANCA).
-
A.
Wegener's granulomatosis
Wegener's granulomatosis, now more commonly called granulomatosis with polyangiitis, is a rare autoimmune disease characterized by inflammation of blood vessels that can damage organs such as the lungs, kidneys, and upper respiratory tract.
-
B.
PR3-ANCA
PR3-ANCA is an autoantibody directed against proteinase 3 that is strongly associated with granulomatosis with polyangiitis (formerly Wegener's granulomatosis) and used as a key diagnostic marker for this vasculitic disease.
-
C.
Behçet's disease
Behçet's disease is a rare, chronic inflammatory disorder characterized by recurrent mouth and genital ulcers, eye inflammation, and systemic vasculitis affecting multiple organ systems.
-
D.
erythema nodosum
Erythema nodosum is an inflammatory condition characterized by tender red nodules, usually on the shins, often associated with systemic diseases such as infections, autoimmune disorders, and inflammatory bowel disease.
-
E.
Behçet
Behçet is a Turkish surname most notably associated with dermatologist Hulusi Behçet, after whom Behçet's disease is named.
- 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_69d6aa9983c08190b0ef61603b69feac |
completed | April 8, 2026, 7:20 p.m. |
| NER | Named-entity recognition | batch_69d7994e32fc8190a6591d9e82b68f75 |
completed | April 9, 2026, 12:19 p.m. |
| NED1 | Entity disambiguation (via context triple) | batch_69e3c8cc77988190aad54f56dbd0f8cf |
completed | April 18, 2026, 6:09 p.m. |
| NEDg | Description generation | batch_69e3cefc00148190a1850dc6e31523c3 |
completed | April 18, 2026, 6:35 p.m. |
| NED2 | Entity disambiguation (via description) | batch_69e3d014a644819092c76aa02b573ca9 |
completed | April 18, 2026, 6:40 p.m. |
Created at: April 8, 2026, 9:26 p.m.