
ncats-arax
Queries the NCATS Translator ARAX production API for bounded, typed, provenance-rich one-hop and endpoint-pinned two-hop biomedical knowledge-graph relationships. Use for Biolink-constrained RTX-KG2 lookup, explicit selected-provider ARAX federation, separate entity normalization, qualifier-aware graph traversal, and inspection of TRAPI edge bindings, publications, and knowledge-source provenance. Do not use for inference, ranking, open-ended pathfinding, clinical guidance, or sensitive queries.
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Install
Works with every agent the skills CLI supports.
npx skills add https://github.com/k-dense-ai/scientific-agent-skills --skill ncats-arax- 01
Install
Run the command in your project. The CLI asks which agents to install for.
- 02
Describe the task
Ask your agent for something this skill covers. It loads ncats-arax automatically when relevant.
- 03
Review the result
The agent follows the SKILL.md steps, scripts and references bundled with the skill.
SKILL.md
The instructions your agent reads when the skill is triggered.
NCATS ARAX
Use ARAX as a constrained knowledge-graph lookup service. Submit reviewed CURIEs and explicit Biolink types, preserve the exact TRAPI exchange, inspect query-edge bindings and provenance, and treat every returned path as a candidate for subsequent verification.
Read query-contract.md before constructing a query. Read output-schema.md when interpreting saved artifacts, warnings, provenance, or partial results.
Safety boundary
- Use only public, nonsensitive research questions. ARAX status facilities may expose query and
caller metadata even when
store=falseis requested. - Do not submit patient information, confidential research questions, unpublished compound programs, or proprietary target hypotheses.
- Do not present a returned path as a validated mechanism or clinical recommendation.
- Report a zero as "not returned under these constraints," never as evidence that no relationship exists.
- Describe position as unscored response order, never rank.
- Verify important candidates with literature and authoritative databases separately.
Workflow
- Normalize free text separately, then review and report the proposed CURIE and category.
- Choose a typed one-hop query or an exactly two-hop query with both endpoints pinned.
- Use default RTX-KG2 lookup unless the user explicitly names two to five providers.
- Acknowledge that the biomedical query is public and choose a new or empty output directory.
- Run the client once. Do not silently change provider selection or expansion order after a failure or empty result.
- Inspect
summary.jsonfor bounded bindings and provenance andresponse.jsonfor the exact TRAPI payload. - Verify scientifically important paths outside ARAX.
Preflight
Check the production OpenAPI without making a biomedical query:
python skills/ncats-arax/scripts/arax_client.py preflight
The client verifies that the service identifies itself as ARAX, exposes POST /query and
GET /entity, and reports a supported TRAPI version. It reads info.x-trapi.version, falling back
to the title for older OpenAPI documents. A nonproduction endpoint or untested TRAPI series
requires an explicit override; neither override changes the fixed query shapes or operations.
Normalize an entity
Normalization is review-only and never triggers a graph query:
python skills/ncats-arax/scripts/arax_client.py normalize "ivacaftor" \
--expected-category biolink:SmallMolecule \
--max-synonyms 10 \
--acknowledge-public-query \
--output-dir outputs/normalize-ivacaftor
Review the canonical identifier, name, category, and synonym preview before using a CURIE. Report
all CURIEs and categories regardless of query outcome. A category warning or zero result is a
reason to curate the identifier, not to chain automatically to /query.
One-hop lookup
Pin at least one endpoint and type both nodes:
python skills/ncats-arax/scripts/arax_client.py one-hop \
--subject-id CHEBI:31690 \
--subject-category biolink:SmallMolecule \
--predicate biolink:affects \
--object-id NCBIGene:25 \
--object-category biolink:Gene \
--qualifier biolink:object_aspect_qualifier=activity_or_abundance \
--qualifier biolink:object_direction_qualifier=decreased \
--acknowledge-public-query \
--output-dir outputs/imatinib-abl1
Lookup mode is the default and fixes expansion to infores:rtx-kg2. It defaults to 20 results.
Use --result-limit N to request 1-50 results; 50 is the hard cap in either mode.
Endpoint-pinned two-hop lookup
Use exactly one typed, unpinned intermediate node:
python skills/ncats-arax/scripts/arax_client.py two-hop \
--subject-id CHEBI:66901 \
--subject-category biolink:SmallMolecule \
--predicate-1 biolink:affects \
--intermediate-category biolink:Gene \
--predicate-2 biolink:associated_with \
--object-id MONDO:0009061 \
--object-category biolink:Disease \
--qualifier-1 biolink:object_aspect_qualifier=activity_or_abundance \
--qualifier-1 biolink:object_direction_qualifier=increased \
--expand-order right-first \
--acknowledge-public-query \
--output-dir outputs/ivacaftor-cystic-fibrosis
Right-first expansion is the default. If an empty result merits another attempt, run a new query
explicitly with --expand-order left-first and keep the runs separate.
Selected-provider federation
Federation is explicit and accepts two to five named providers:
python skills/ncats-arax/scripts/arax_client.py one-hop \
--subject-id CHEBI:31690 \
--subject-category biolink:SmallMolecule \
--predicate biolink:affects \
--object-id NCBIGene:25 \
--object-category biolink:Gene \
--mode federated \
--kp infores:rtx-kg2 \
--kp infores:molepro \
--acknowledge-public-query \
--output-dir outputs/federated-imatinib-abl1
Federation defaults to the hard maximum of 50 results. Provider errors may coexist with useful results; such a run exits 7 after retaining its artifacts and is marked partial. The same applies to a failed provider in lookup mode. An explicit non-success ARAX response status exits 6 with the raw response retained; it must not be reported as a successful zero-result query.
Inspect saved provenance
Rebuild a bounded summary without network access:
python skills/ncats-arax/scripts/arax_client.py summarize \
--request outputs/ivacaftor-cystic-fibrosis/request.json \
--response outputs/ivacaftor-cystic-fibrosis/response.json \
--format text
The inspector accepts only the same constrained request shapes and fixed operations that the live
commands generate. Use --format json for the normalized view on standard output.
Interpret results
- Follow each analysis's query-edge bindings; do not summarize every knowledge-graph edge.
- Preserve the physical edge subject, predicate, object, and qualifier values returned by ARAX. Returned predicates or qualifier aspects may be more specific than the query constraint.
- Inspect all source objects, including primary, aggregator, supporting-data, upstream-resource, and source-record URL fields.
- Trace aggregator edges to their primary/upstream sources and publications before claiming corroboration. Multiple providers can redistribute the same record; report distinct primary evidence, not provider count as confidence or independent replication.
- Treat
publication_availability: not_returnedas missing metadata, not evidence that no publications exist. - Treat missing auxiliary-graph references and provider failures as explicit warnings.
- Consult the raw response whenever the bounded summary omits detail or the service response is partial, unfamiliar, or scientifically surprising.
Deliberate exclusions
The client has no raw-query, workflow, operation, overlay, ranking, inference, link-prediction, Pathfinder, ARS, batch, all-provider, three-hop, cache, daemon, SDK, MCP, or natural-language-to-TRAPI surface. Do not work around those limits with direct HTTP calls under this skill.
Official references
Reviewed on 2026-09-30 against production ARAX 1.5.4 / TRAPI 1.5.0 (the URL still contains v1.4).
Live public smoke tests passed for preflight, normalization, qualified one-hop and endpoint-pinned
two-hop lookups, and RTX-KG2/MolePro federation. Results and provider availability can change.
The official introductory guide contains older response examples; use the deployed schema and
current ARAX source for field and operation contracts. No Python SDK is used by this client.
FAQ
What does the ncats-arax skill do?
Queries the NCATS Translator ARAX production API for bounded, typed, provenance-rich one-hop and endpoint-pinned two-hop biomedical knowledge-graph relationships. Use for Biolink-constrained RTX-KG2 lookup, explicit selected-provider ARAX federation, separate entity normalization, qualifier-aware graph traversal, and inspection of TRAPI edge bindings, publications, and knowledge-source provenance. Do not use for inference, ranking, open-ended pathfinding, clinical guidance, or sensitive queries.
How do I install ncats-arax?
Run npx skills add https://github.com/k-dense-ai/scientific-agent-skills --skill ncats-arax in your project. The skills CLI detects the agents you use and copies the skill into the right folder. For Claude Code you can also place the skill folder at ~/.claude/skills/ncats-arax/ (personal) or .claude/skills/ncats-arax/ (project).
Which AI agents can use ncats-arax?
Any agent that supports the open Agent Skills format (a folder with a SKILL.md file), including Claude Code, Codex, Cursor, GitHub Copilot, Gemini CLI, Windsurf, Cline, OpenCode and more.
Is ncats-arax safe to install?
No partner security audit is available yet. Skills can run commands and scripts, so read the SKILL.md and any bundled files before installing.
Who maintains ncats-arax?
It is published by k-dense-ai in k-dense-ai/scientific-agent-skills. It has 882 recorded installs.
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