Aug 2026· Artif. Intell. Medicine· Vol 181, pp.
103510
· 0 citations· 86 references
MedicineComputer Science
TL;DR
Link prediction validated PregBase's inference capability beyond extracted knowledge, recovering established clinical interventions, reconstructing canonical hormonal pathways across maternal-placental-fetal compartments, and identifying novel biomarker candidates for preterm birth, gestational diabetes, and preeclampsia.
Abstract
Pregnancy complications are a leading cause of maternal and neonatal mortality worldwide. Understanding their underlying mechanisms is hindered by dispersed evidence across thousands of studies and complex biological interactions. We present PregBase, a comprehensive knowledge base for pregnancy research comprising automated extraction, validation, and exploration. PregBase was constructed by utilising large language models (LLMs) to extract relationships from literature; 13 LLMs were benchmarked across seven prompting strategies, with ensemble shuffle prompting outperforming single-strategy alternatives. A three-tier validation pipeline combining ontology mapping, graph neural networks, and statistical analysis produced PregKG, a knowledge graph containing 64,087 associations between 13,303 biomedical entities spanning 155 semantic types and 50 vocabularies across 8 relationship types from 8420 articles. Link prediction validated PregBase's inference capability beyond extracted knowledge, recovering established clinical interventions, reconstructing canonical hormonal pathways across maternal-placental-fetal compartments, and identifying novel biomarker candidates for preterm birth, gestational diabetes, and preeclampsia, supported by genetic and expression databases. An interactive web interface (https://pregknowledgebase.com) has been created to enable further exploration via conversational queries. This work provides a scalable foundation for systematic discovery in maternal health research.
Background Phenotype-genotype associations underpin precision medicine by enabling disease prevention, early diagnosis, risk stratification, therapeutic target discovery, and personalized treatment. However, the rapid growth of scientific evidence has made manual curation of these associations increasingly labor-intens...
Caiwan Sun, Yi Xin, Sarah Zeng et al.· bioRxiv· 0 citations
By unifying fragmented research and enabling robust data exploration, UKB-KG emerges as a powerful tool for advancing biomedical research and driving innovative healthcare applications.
Z. Wang, J. Wang, Y. Shen et al.· medRxiv· 0 citations
A conceptual framework and roadmap for addressing four interrelated translational failure domains through rigorous validation, uncertainty-aware methods, interoperable infrastructures, regulatory alignment, and human oversight across the AI lifecycle is proposed.
Bahar Ilgen, Yiannos S. Tolias, D. Kühnert et al.· 0 citations
This work presents a scalable, reproducible framework for evaluating, optimizing, and interpreting LLMs for biomedical knowledge extraction, with a focus on gene–gene regulatory relation prediction, pathway component recognition, multimodal pathway figure understanding, and automated prompt optimization.
Most clinical prediction systems learn patient-variable-outcome associations; we investigate a training-free diagnostic paradigm mapping patient observations to explicit medical knowledge. CKG Reasoner integrates candidate-specific Evidence Feature Nodes, patient-reference matching, a bounded Information Gate, knowledg...
A framework for evaluating the translational impact of the Gabriella Miller Kids First Program enables systematic assessment of how research investments contribute to clinically actionable knowledge and translational impact, providing a model for evaluating future precision medicine and pediatric oncology research init...
Vanessa I. Barnes· Cancer Research· 0 citations
We use cookies to run the site and, with your consent, for analytics and to show ads.
See our Cookie Policy.