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A transition-based model for jointly extracting drugs, diseases and adverse drug events

机译:基于过渡的模型,用于联合提取毒品,疾病和不良药品事件

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Extracting adverse drug events (a.k.a. drug-induced diseases or drug side effects) from the raw text has been widely studied in the biomedical area. It is usually assumed that entities of drugs and diseases are given by a separated named entity recognition model. In this paper, we propose a joint model to extract drugs, diseases and adverse drug events simultaneously. In our model, the structured perceptron is leveraged for training and multiple-beam search algorithm is used for decoding. The search algorithm is transition-based, i.e., an input sentence is processed in left-to-right order and predefined actions transit the sentence from one state to another which corresponds to a predicted result about drugs, diseases and adverse drug events in that sentence. Experimental results show that our joint approach obtains comparable performance compared with the baseline or state-of-the-art approaches and achieves 55.20% precision, 47.97% recall and 51.14% F1-measure in extraction of adverse drug events. We demonstrate that the joint approach is effective and can be easily extended to other entity-relation extraction systems such as protein-protein interactions and gene-disease relations. To facilitate the related research, our code is available online at: https://github.com/foxlf823/ade.
机译:从原始文本中提取不良药物事件(亦称药物引起的疾病或药物副作用)已在生物医学领域得到了广泛研究。通常假设药物和疾病的实体是由单独的命名实体识别模型给出的。在本文中,我们提出了一个联合模型来同时提取药物,疾病和不良药物事件。在我们的模型中,结构化感知器用于训练,而多波束搜索算法用于解码。搜索算法基于过渡,即按从左到右的顺序处理输入的句子,并且预定义的动作将句子从一个状态转移到另一状态,这对应于该句子中有关毒品,疾病和药物不良事件的预测结果。实验结果表明,我们的联合方法与基线方法或最新方法相比具有可比的性能,并且在提取不良药物事件中达到了55.20%的精度,47.97%的召回率和51.14%的F1量度。我们证明了联合方法是有效的,可以很容易地扩展到其他实体关系提取系统,例如蛋白质-蛋白质相互作用和基因-疾病关系。为了促进相关研究,我们的代码可从以下位置在线获得:https://github.com/foxlf823/ade。

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