摘要
Orphanet是欧盟委员会支持的研究项目之一,目前它已发展为一个多达37个国家的巨大网络,其成员国遍及全球.在此数据库中我们可查询到罕见病的临床体征、基因、分类、罕见病的药物数据集以及最新发现的罕见病和与之对应的研究报道、研究机构和专家信息.它是有关罕见病不可多得的一种独特资源,具有实时收集和更新有关罕见病知识的功能,从而改善对罕见病患者的诊断,护理和治疗.本文是对Orphanet背景简单的介绍,以及对不同模块的数据集挖掘进行指引.
Orphanet is one of the research projects supported by the European Commission.At present,it has developed into a huge network of up to 37 countries,and its member countries span the globe.In this database,we can query the clinical signs,genes,classifications of rare diseases,drug data sets of rare diseases,and the latest discovered rare diseases and corresponding research reports,research institutions and expert information.It is a unique resource about rare diseases and has the function of collecting and updating knowledge about rare diseases in real time,thereby improving the diagnosis,care and treatment of patients with rare diseases.This article is a brief introduction to the background of Orphanet,and a guide to data mining of different modules.
作者
郑帅
田国祥
韩迪迪
李承倬
许丰硕
吕军
Zheng Shuai;Tian Guoxiang;Han Didi;Li Chengzhuo;Xu Fengshuo;Lyu Jun(School of Public Health,Shaanxi University of Chinese Medicine,Xianyang,712046,People's Republic of China;不详)
出处
《中国循证心血管医学杂志》
2020年第6期651-654,共4页
Chinese Journal of Evidence-Based Cardiovascular Medicine
基金
国家社会科学基金一般项目(16BGL183)。
