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

机译:共同提取药物,疾病和不良药物事件的转型模型

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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:从生物医学区域中广泛研究了从原始文本中提取不良药物(A.K.A.药物诱导的疾病或药物副作用)。通常假设药物和疾病的实体由分离的命名实体识别模型给出。在本文中,我们提出了一个联合模型,同时提取药物,疾病和不良药物事件。在我们的模型中,用于训练的结构化的Perceptron和多梁搜索算法用于解码。搜索算法是基于转换的,即,在左右顺序处理输入句子,并且预定义操作将句子从一个状态传输到另一个状态,这对应于该句子中的药物,疾病和不良药物事件的预测结果。实验结果表明,与基线或最先进的方法相比,我们的联合方法获得了相当的性能,并达到了55.20%的精度,47.97%的召回和51.14%的F1 - 衡量不良药物事件的措施。我们表明,联合的方式是有效的,可以很容易地扩展到其他实体关系抽取系统,如蛋白质 - 蛋白质相互作用和基因疾病的关系。为方便相关研究,我们的代码可在线提供:https://github.com/foxlf823/ade。

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