S2CIE: semantic, syntactic, and context-based information extraction for AOP development

Adverse Outcome Pathways (AOPs) provide a structured framework for linking mechanistic events across biological organization levels, supporting chemical hazard identification and regulatory decision-making in Next-Generation Risk Assessment (NGRA). However, AOP development remains labor-intensive, requiring extensive literature searching and expert review to identify relevant events and supporting evidence. Existing text mining tools often operate on limited datasets, lack interactive capabilities, and miss contextually relevant studies. To address these challenges, we present S<sup>2</sup>CIE (Semantic & Syntactic Context-based Information Extraction), an interactive, real-time platform for extracting mechanistic information from biomedical literature. S<sup>2</sup>CIE annotates PubMed abstracts (32 million) at the word level with grammatical, entity-type, and dependency annotations, enabling custom extraction rules based on syntactic patterns, and employ semantic retrieval based on user specific query. The system supports near real-time querying and integrates entity recognition and visual exploration tools. We demonstrate S<sup>2</sup>CIE's utility through four case studies. First, we identified 110 chemicals linked to liver steatosis/cholestasis with 98.79% precision, extracting chemical and PPAR (peroxisome proliferator-activated receptors) interactions as molecular initiating events. Second enrichment analysis of literature derived genes and successful mapping with AOPs. Third, comparative analysis against AOP-HelpFinder for key event relationships in AOP 220 showed 42.2% increased evidence capture (1,614 vs 1,135 abstracts) with 99% reduced retrieval time. Fourth, large-scale extraction of post-translational modification events demonstrated domain-agnostic applicability beyond toxicology. S<sup>2</sup>CIE accelerates AOP evidence gathering, while maintaining transparency and auditability essential for regulatory application. S<sup>2</sup>CIE is available as open source through an API and as web application at https://dev.s2cie.insilicohub.org/.

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Publication Details

Journal
Environment International
Published
2025-12-06
DOI
https://doi.org/10.1016/j.envint.2025.109986
Primary Topic
Biomedical Text Mining and Ontologies
Type
article
Field-Weighted Citation Impact
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article

S2CIE: semantic, syntactic, and context-based information extraction for AOP development

Vikas Kumar, Saurav Kumar, Deepika Deepika, Antonio Moreno et al.
Environment International
Biomedical Text Mining and Ontologies
article

S2CIE: semantic, syntactic, and context-based information extraction for AOP development

Vikas Kumar, Saurav Kumar, Deepika Deepika, Antonio Moreno, Shubh Sharma, Judit Biosca-Brull
article en

Abstract

Adverse Outcome Pathways (AOPs) provide a structured framework for linking mechanistic events across biological organization levels, supporting chemical hazard identification and regulatory decision-making in Next-Generation Risk Assessment (NGRA). However, AOP development remains labor-intensive, requiring extensive literature searching and expert review to identify relevant events and supporting evidence. Existing text mining tools often operate on limited datasets, lack interactive capabilities, and miss contextually relevant studies. To address these challenges, we present S<sup>2</sup>CIE (Semantic & Syntactic Context-based Information Extraction), an interactive, real-time platform for extracting mechanistic information from biomedical literature. S<sup>2</sup>CIE annotates PubMed abstracts (32 million) at the word level with grammatical, entity-type, and dependency annotations, enabling custom extraction rules based on syntactic patterns, and employ semantic retrieval based on user specific query. The system supports near real-time querying and integrates entity recognition and visual exploration tools. We demonstrate S<sup>2</sup>CIE's utility through four case studies. First, we identified 110 chemicals linked to liver steatosis/cholestasis with 98.79% precision, extracting chemical and PPAR (peroxisome proliferator-activated receptors) interactions as molecular initiating events. Second enrichment analysis of literature derived genes and successful mapping with AOPs. Third, comparative analysis against AOP-HelpFinder for key event relationships in AOP 220 showed 42.2% increased evidence capture (1,614 vs 1,135 abstracts) with 99% reduced retrieval time. Fourth, large-scale extraction of post-translational modification events demonstrated domain-agnostic applicability beyond toxicology. S<sup>2</sup>CIE accelerates AOP evidence gathering, while maintaining transparency and auditability essential for regulatory application. S<sup>2</sup>CIE is available as open source through an API and as web application at https://dev.s2cie.insilicohub.org/.

Environment InternationalVol. 207
Institut de Recerca Biomèdica Catalunya Sud (ES), Universitat Rovira i Virgili (ES)
Openalex Percentile: Top 65%
Biomedical Text Mining and Ontologies
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