[nxontology-ml] Sample precision prompt

gistfile1.txt

A list of records will be provided from an ontology of disease terms. Each record will contain information describing a single term.

Assign a `precision` label to each of these terms that captures the extent to which they correspond to patient populations with distinguishing clinical, demographic, physiological or molecular characteristics. Use exactly one of the following values for this label:

- `high`: High precision terms have the greatest ontological specificity, sometimes (but not necessarily) correspond to small groups of relatively homogeneous patients, often have greater diagnostic certainty and typically represent the forefront of clinical practice.
- `medium`: Medium precision terms are the ontological ancestors of `high` precision terms (if any are known), often include indications in later stage clinical trials and generally reflect groups of patients assumed to be suffering from a condition with a shared, or at least similar, physiological or environmental origin.
- `low`: Low precision terms are the ontological ancestors of both `medium` and `high` precision terms, group collections of diseases with *some* shared characteristics and typically connote a relatively heterogenous patient population. They are often terms used within the ontology for organizational purposes.

The records provided will already have the following fields:

- `id`: A string identifier for the term
- `label`: A descriptive name for the term
- `description`: A longer, possibly truncated description of what the term is; may be NA (i.e. absent)

Here is a list of such records (in YAML format) where the `precision` label is already assigned for 3 examples at each level of precision:

--- BEGIN EXAMPLES ---
- id: EFO:1000639
  label: acquired metabolic disease
  definition: A disease of metabolism that has _material_basis_in enzyme deficiency or accumulation of enzymes or toxins which interfere with normal function due to an endocrine organ disease, organ malfunction, inadequate intake, dietary deficiency, or ...
  precision: low
- id: Orphanet:68336
  label: Rare genetic tumor
  definition: NA
  precision: low
- id: EFO:0005548
  label: developmental disorder of mental health
  definition: A disease of mental health that occur during a child’s developmental period between birth and age 18 resulting in retarding of the child’s
  precision: low
- id: EFO:0005548
  label: inflammatory bowel disease
  definition: A spectrum of small and large bowel inflammatory diseases of unknown etiology. It includes Crohn's disease, ulcerative colitis, and colitis of indeterminate type.
  precision: medium
- id: EFO:0000384
  label: Crohn's disease
  definition: A gastrointestinal disorder characterized by chronic inflammation involving all layers of the intestinal wall, noncaseating granulomas affecting the intestinal wall and regional lymph nodes, and transmural fibrosis. Crohn disease most ...
  precision: medium
- id: MONDO:0045020
  label: glycine metabolism disease
  definition: A disease that has its basis in the disruption of glycine metabolic process.
  precision: medium
- id: EFO:1000277
  label: Gastric Small Cell Neuroendocrine Carcinoma
  definition: An aggressive, high-grade and poorly differentiated carcinoma with neuroendocrine differentiation that arises from the stomach. It is characterized by the presence of malignant small cells.
  precision: high
- id: MONDO:0015634
  label: isolated osteopoikilosis
  definition: A osteopoikilosis (disease) that is not part of a larger syndrome.
  precision: high
- id: Orphanet:98755
  label: Spinocerebellar ataxia type 1
  definition: Spinocerebellar ataxia type 1 (SCA1) is a subtype of type I autosomal dominant cerebellar ataxia (ADCA type I; see this term) characterized by dysarthria, writing difficulties, limb ataxia, and commonly nystagmus and saccadic abnormalities.
  precision: high
--- END EXAMPLES ---

Here are the records for which this `precision` label is not yet known:

--- BEGIN RECORDS ---
- id: DOID:0050890
  label: synucleinopathy
  definition: A neurodegenerative disease that is characterized by the abnormal accumulation of aggregates of alpha-synuclein protein in neurons, nerve fibres or glial cells. [url:http://en.wikipedia.org/wiki/Synucleinopathies ]
- id: EFO:0006792
  label: Lewy body dementia
  definition: A progressive form of dementia characterized by the presence of protein deposits called Lewy bodies in the midbrain and cerebral cortex, and loss of cholinergic and dopaminergic neurons. The signs and symptoms overlap with Alzheimer and Parkinson disease.
--- END RECORDS ---

Requirements:

- Assign a `precision` label for ALL records
- Respond in CSV format using a pipe (i.e. "|") delimiter with the headers `id`, `precision` where `id` is the `id` associated with each record
- Include the headers in the result
- Respond with ONLY the CSV content, do not include explanation of any kind

CSV: