LORE:规模化疾病基因致病性预测的文献语义框架

P.-H. Li, Y.-Y. Sun, H.-F. Juan, C.-Y. Chen, H.-K. Tsai, J.-H. Huang
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引用次数: 0

摘要

有效利用学术文献对于机器阅读理解产生可操作的科学知识以广泛应用于现实世界至关重要。最近,大语言模型(LLM)已成为从科学文章中提炼知识的有力工具,但它们在可靠性和可验证性问题上举步维艰。在这里,我们提出了一种新颖的无监督两阶段阅读方法--LORE,它将文献建模为可验证事实陈述的知识图谱,并反过来将其建模为欧几里得空间中的语义嵌入。将 LORE 应用于 PubMed 摘要,以大规模了解疾病-基因关系,从而捕捉到基因致病性的基本信息。此外,我们还证明,通过 ClinVar 数据库的监督,在语义嵌入中建立潜在致病流模型,可在 2,097 种疾病中识别相关基因,平均精确度达到 90%。最后,我们创建了一个具有预测致病性得分的疾病-基因关系知识图谱,其规模是 ClinVar 数据库的 200 倍。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
LORE: A Literature Semantics Framework for Evidenced Disease-Gene Pathogenicity Prediction at Scale
Effective utilization of academic literature is crucial for Machine Reading Comprehension to generate actionable scientific knowledge for wide real-world applications. Recently, Large Language Models (LLMs) have emerged as a powerful tool for distilling knowledge from scientific articles, but they struggle with the issues of reliability and verifiability. Here, we propose LORE, a novel unsupervised two-stage reading methodology with LLM that models literature as a knowledge graph of verifiable factual statements and, in turn, as semantic embeddings in Euclidean space. Applied to PubMed abstracts for large-scale understanding of disease-gene relationships, LORE captures essential information of gene pathogenicity. Furthermore, we demonstrate that modeling a latent pathogenic flow in the semantic embedding with supervision from the ClinVar database leads to a 90% mean average precision in identifying relevant genes across 2,097 diseases. Finally, we have created a disease-gene relation knowledge graph with predicted pathogenicity scores, 200 times larger than the ClinVar database.
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