Gene-disease association analysis across DisGeNET, OpenTargets, Monarch, OMIM, GenCC, Orphanet. Cross-references multiple sources for evidence-graded association reports with concordance scoring (5/5 sources agree → strong, 1/5 → weak). Use for 'which diseases is gene X associated with' or 'which genes cause disease Y' queries with quantitative confidence.
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Low
Low-risk findings worth noting
Low
Low-risk findings.
1 low severity finding. Worth noting, but not necessarily harmful.
The skill exposes the agent to untrusted, user-generated content from public third-party sources, creating a risk of indirect prompt injection. This includes browsing arbitrary URLs, reading social media posts or forum comments, and analyzing content from unknown websites.
The workflow ingests outsider-authored free text at runtime only via its external database/API queries (e.g., DisGeNET/OMIM/OpenTargets/Monarch/ClinVar), but the required workflow itself is driven by user-supplied gene/disease identifiers rather than by reading arbitrary user-submitted content streams or selecting specific attacker-authored items first.
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