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首页> 外文期刊>Journal of biomedical informatics. >Combining automatic table classification and relationship extraction in extracting anticancer drug-side effect pairs from full-text articles
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Combining automatic table classification and relationship extraction in extracting anticancer drug-side effect pairs from full-text articles

机译:从全文文章中结合自动表分类和关系提取在提取抗癌药物侧效对

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Anticancer drug-associated side effect knowledge often exists in multiple heterogeneous and complementary data sources. A comprehensive anticancer drug-side effect (drug-SE) relationship knowledge base is important for computation-based drug target discovery, drug toxicity predication and drug repositioning. In this study, we present a two-step approach by combining table classification and relationship extraction to extract drug-SE pairs from a large number of high-profile oncological full-text articles. The data consists of 31,255 tables downloaded from the Journal of Oncology (JCO). We first trained a statistical classifier to classify tables into SE-related and -unrelated categories. We then extracted drug-SE pairs from SE-related tables. We compared drug side effect knowledge extracted from JCO tables to that derived from FDA drug labels. Finally, we systematically analyzed relationships between anti-cancer drug-associated side effects and drug-associated gene targets, metabolism genes, and disease indications. The statistical table classifier is effective in classifying tables into SE-related and -unrelated (precision: 0.711; recall: 0.941; F1: 0.810). We extracted a total of 26,918 drug-SE pairs from SE-related tables with a precision of 0.605, a recall of 0.460, and a Fl of 0.520. Drug-SE pairs extracted from JCO tables is largely complementary to those derived from FDA drug labels; as many as 84.7% of the pairs extracted from JCO tables have not been included a side effect database constructed from FDA drug labels. Side effects associated with anticancer drugs positively correlate with drug target genes, drug metabolism genes, and disease indications. (C) 2014 Elsevier Inc. All rights reserved.
机译:抗癌药物相关的副作用知识通常存在于多种异构和互补的数据源中。全面的抗癌药物副作用(药物-E)关系知识库对于基于计算的药物目标发现,药物毒性预测和药物重新定位是重要的。在这项研究中,我们通过组合表分类和关系提取来提取两步方法,以从大量高调的肿瘤内全文制品中提取药物-SE对。数据包括从肿瘤学杂志(JCO)下载的31,255张表格组成。我们首先培训了一个统计分类器,将表对与相关的和 - 许多类分类。然后我们从相关表中提取药物-SE对。我们比较了从JCO表中提取的药物副作用知识,从FDA药物标签中衍生出来。最后,我们系统地分析了抗癌药物相关副作用和药物相关基因靶,代谢基因和疾病指示之间的关系。统计表分类器有效地将表分类为相关的和 - 不合适(精确:0.711;召回:0.941; F1:0.810)。我们通过精度从SE相关表中提取了26,918个药物-SE对,精度为0.605,召回0.460,FL为0.520。从JCO表中提取的药物-SE对主要与来自FDA药物标签的那些互补;从JCO表中提取的,多达84.7%未包含由FDA药物标签构成的副作用数据库。与抗癌药物相关的副作用与药物靶基因,药物代谢基因和疾病适应症呈正相关。 (c)2014年elsevier Inc.保留所有权利。

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