Skill UI

This skill programmatically searches and fetches biomedical literature from PubMed and PMC using NCBI E-utilities (ESearch, EFetch, ESummary). It allows users to gather large corpora of abstracts, full texts, and metadata related to specific conditions, drugs, or genes. Ideal for building evidence bases, performing biomedical Named Entity Recognition (NER), or summarizing scientific findings.

This skill standardizes free-text medication mentions extracted by OpenMed to RxNorm RxCUIs using the public RxNav API. It resolves complex relationships between brand names, generic ingredients, strengths, and dose forms, providing a stable, canonical code. Ideal for clinical interoperability, data analytics, de-duplication, and building US Core Medication resources.

A comprehensive guide for installing, configuring, and validating the local long-term memory plugin (`memory-tencentdb`) within the OpenClaw environment. This guide covers everything from environment pre-checks to advanced configuration for data capture, information extraction, context recall, and vector embedding, ensuring robust, self-contained memory capabilities for RAG applications.

This skill parses standardized C-CDA/CCD XML clinical documents exported from EHRs. It extracts both human-readable section narrative text and coded entries, mapping them by LOINC codes and template IDs. It is essential for preparing clinical free-text data for subsequent NLP analysis and supports XML-aware de-identification while preserving document structure.

This skill processes clinical text to interpret laboratory results. It parses reference ranges (e.g., "135-145", "<5") and derives structured abnormal flags (low, normal, high, critical) for a given numeric value. It is unit-agnostic and respects explicit flags provided by the originating lab, making it crucial for structured clinical data extraction and interpretation workflows.

This skill parses complex, free-text clinical trial eligibility criteria from sources like ClinicalTrials.gov into structured, machine-readable rules. It then evaluates these criteria against a comprehensive patient profile (derived from OpenMed data) to determine potential eligibility. The output provides an explainable verdict (eligible, ineligible, or unknown) for every criterion, serving as a critical decision support tool for clinicians and researchers.

This skill connects extracted drug entities with authoritative regulatory facts from the public OpenFDA API. It retrieves Structured Product Labeling (SPL) data, NDC package codes, approved indications, boxed warnings, and current recall/enforcement status. It is essential for enriching drug profiles, providing regulatory context, and supporting unexpectedness checks. Note: This skill provides information, not clinical decision support.

This skill facilitates the crucial grounding step for clinical coding by interacting with external FHIR terminology servers. It supports core operations such as `$validate-code`, `$expand` (for ValueSets), `$lookup`, and `$translate` (ConceptMaps). It ensures that raw text spans are converted into validated, coded `CodeableConcept` resources using industry standards like SNOMED CT, LOINC, and ICD-10, maintaining interoperability.

A robust template designed for creating complex, multi-stage commands or 'recipes.' It enforces a highly structured process by mandating 'Context Validation Checkpoints' before any step executes. This pattern ensures that preconditions are explicitly verified, significantly increasing the reliability and predictability of complex automated workflows.

This skill facilitates reversible de-identification (pseudonymization) of clinical text, allowing sensitive Protected Health Information (PHI) to be masked for processing while retaining the ability to restore the original data later under strict authorization. It captures a mapping key and provides a function to re-identify the text, crucial for workflows like GDPR compliance, patient recontact, or auditing. Crucially, the re-identification mapping must be stored separately and securely.

This skill structures free-text adverse event narratives into the mandatory ICH E2B(R3) format. It populates critical fields required for regulatory submissions (like FAERS/EudraVigilance), including suspect drugs, reactions (mapped via MedDRA), seriousness criteria, and reaction outcomes. Use it when generating Individual Case Safety Reports (ICSRs) from clinical narratives.

This skill enhances raw clinical entity recognition by assigning three critical axes: Negation, Temporality, and Uncertainty (ConText). It determines the clinical status of a mention (e.g., affirmed, negated, historical, or uncertain), ensuring that basic NER results are transformed into clinically faithful assertions before grounding to standards like FHIR. Essential for accurate problem list generation and differential diagnosis support.