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数据分析与知识发现  2022, Vol. 6 Issue (7): 87-98     https://doi.org/10.11925/infotech.2096-3467.2021.1364
  研究论文 本期目录 | 过刊浏览 | 高级检索 |
基于多源语义知识图谱的药物知识发现:以药物重定位为实证*
张晗(),安欣宇,刘春鹤
中国医科大学健康管理学院 沈阳 110122
Building Multi-Source Semantic Knowledge Graph for Drug Repositioning
Zhang Han(),An Xinyu,Liu Chunhe
School of Health Management, China Medical University, Shenyang 110122, China
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摘要 

目的】探讨全数据集、跨数据平台的语义知识图谱构建方法,开展基于知识图谱的药物知识发现研究。【方法】获取PubMed、DrugBank、CTD等数据库的知识关联,通过知识融合、属性定义构建语义知识图谱,以药物重定位为实证,采用路径搜索和链路预测两种方法推理药物在肿瘤治疗中的新用途。【结果】利用知识图谱能有效地进行药物发现,两种方法的总体预测效果相近,路径发现预测F值为0.57, 略高于链路预测(0.56)。此外,药物与适应症之间存在的路径数越多,预测阳性的可能性越大。【局限】 实证研究知识推理机制建立在已有知识关联基础上,难以对无靶点信息的新药进行挖掘;同时庞大的数据体量难以实现知识图谱的动态更新。【结论】融合多源数据集构建的知识图谱能有效地发现药物新适应症,提升药物研发效率,为药物知识发现提供新思路。

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张晗
安欣宇
刘春鹤
关键词 知识发现药物重定位语义模型知识图谱    
Abstract

[Objective] This paper constructs a cross-platform semantic knowledge graph with whole datasets, which helps us find novel drug knowledge. [Methods] First, we developed a new model for the proposed knowledge graph, which integrated semantic relations from PubMed, DrugBank and CTD, as well as knowledge fusion and attribute definition. Then, we conducted drug repositioning with pathway identification and link predication to discover new treatments for cancers. [Results] The F-score of pathway identification (0.57) was better than that of the linkage predication (0.56). The more pathways existing between drugs and indications, the greater possibility of predicting positively. [Limitations] Since the reasoning mechanism was based on the existing associations among knowledge units, it is hard to discover the novel indications for drugs without the known targets. It is difficult to update knowledge graph dynamically due to the huge data volume. [Conclusions] The proposed knowledge graph could effectively find new drug indications as well as improve the efficiency for drug research and development.

Key wordsKnowledge Discovery    Drug Repositioning    Semantic Model    Knowledge Graph
收稿日期: 2021-12-01      出版日期: 2022-08-24
ZTFLH:  R9 G353  
基金资助:*辽宁省社会科学规划基金项目的研究成果之一(L19BTQ006)
通讯作者: 张晗,ORCID:0000-0002-9085-5875     E-mail: zhanghan@cmu.edu.cn
引用本文:   
张晗, 安欣宇, 刘春鹤. 基于多源语义知识图谱的药物知识发现:以药物重定位为实证*[J]. 数据分析与知识发现, 2022, 6(7): 87-98.
Zhang Han, An Xinyu, Liu Chunhe. Building Multi-Source Semantic Knowledge Graph for Drug Repositioning. Data Analysis and Knowledge Discovery, 2022, 6(7): 87-98.
链接本文:  
https://manu44.magtech.com.cn/Jwk_infotech_wk3/CN/10.11925/infotech.2096-3467.2021.1364      或      https://manu44.magtech.com.cn/Jwk_infotech_wk3/CN/Y2022/V6/I7/87
Fig.1  药物知识发现图谱构建框架
分类 实体的语义类型
药物(Drug) orch, phsu, bacs, antb, elii, irda, imft, inch
靶点(Target) gngm, aapp
疾病(Disease) acab, anab, comd, agab, dsyn, emod, fndg,
inpo, mobd, neop, patf, sosy
Table 1  知识图谱实体类别-语义类型对照
Fig.2  知识图谱示意
药物 上市时间 最初用途 肿瘤治疗发现时间 发现途径 预测图谱 验证图谱
Itraconazole 1984 真菌感染 2007 小鼠模型 1984-2006 2007-2020
Nelfinavir 1997 HIV感染 2005 临床试验 1997-2004 2005-2020
Digoxin 1947 心脏病 1982 临床试验 1947-1981 1982-2020
Riluzole 1988 肌萎缩侧索硬化症 2009 小鼠模型 1988-2008 2009-2020
Table 2  药物数据概况
Fig.3  预测图谱药物发现搜索路径
方法 药物 预测数 标准数 预测正确数 准确率 召回率 F值
路径发现 Itraconazole 58 35 30 0.52 0.86 0.65
Nelfinavir 46 32 27 0.59 0.84 0.69
Digoxin 10 29 6 0.6 0.21 0.31
Riluzole 34 29 15 0.44 0.52 0.48
汇总 148 125 78 0.53 0.62 0.57
链路预测 Itraconazole 76 35 32 0.42 0.91 0.58
Nelfinavir 36 32 24 0.67 0.75 0.71
Digoxin 5 29 4 0.80 0.14 0.24
Riluzole 50 29 22 0.44 0.76 0.56
汇总 167 125 82 0.49 0.66 0.56
BITOLA Itraconazole 98 35 29 0.30 0.83 0.44
Nelfinavir 80 32 25 0.31 0.78 0.45
Digoxin 100 29 23 0.23 0.79 0.36
Riluzole 87 29 24 0.28 0.83 0.41
汇总 365 125 101 0.28 0.81 0.42
Table 3  药物预测评价结果
药物 LTC- Freq LTC-AMW Freq AMW Adamic Adar
Itraconazole 0.94 0.91 0.87 0.66 0.67
Nelfinavir 0.91 0.91 0.88 0.54 0.86
Digoxin 0.94 0.94 0.73 0.75 0.70
Riluzole 0.74 0.70 0.55 0.44 0.64
Table 4  4种排序方法的MAP
Fig.4  两组疾病与关联靶点分布
Fig.5  伊曲康唑发现结果
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