RDBridge: a knowledge graph of rare diseases based on large-scale text mining

被引:2
作者
Xing, Huadong [1 ]
Zhang, Dachuan [2 ]
Cai, Pengli [1 ]
Zhang, Rui [1 ]
Hu, Qian-Nan [1 ]
机构
[1] Chinese Acad Sci, Univ Chinese Acad Sci, Shanghai Inst Nutr & Hlth, CAS Key Lab Computat Biol, Shanghai 200031, Peoples R China
[2] Swiss Fed Inst Technol, Inst Environm Engn, CH-8093 Zurich, Switzerland
关键词
DATABASE;
D O I
10.1093/bioinformatics/btad440
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
Motivation: Despite low prevalence, rare diseases affect 300 million people worldwide. Research on pathogenesis and drug development lags due to limited commercial potential, insufficient epidemiological data, and a dearth of publications. The unique characteristics of rare diseases, including limited annotated data, intricate processes for extracting pertinent entity relationships, and difficulties in standardizing data, represent challenges for text mining. Results: We developed a rare disease data acquisition framework using text mining and knowledge graphs and constructed the most comprehensive rare disease knowledge graph to date, Rare Disease Bridge (RDBridge). RDBridge offers search functions for genes, potential drugs, pathways, literature, and medical imaging data that will support mechanistic research, drug development, diagnosis, and treatment for rare diseases. Availability and implementation: RDBridge is freely available at http://rdb.lifesynther.com/.
引用
收藏
页数:4
相关论文
共 23 条
[1]  
Davenport Thomas, 2019, Future Healthc J, V6, P94, DOI 10.7861/futurehosp.6-2-94
[2]   Amyotrophic lateral sclerosis [J].
Feldman, Eva L. ;
Goutman, Stephen A. ;
Petri, Susanne ;
Mazzini, Letizia ;
Savelieff, Masha G. ;
Shaw, Pamela J. ;
Sobue, Gen .
LANCET, 2022, 400 (10360) :1363-1380
[3]  
Gupta H., 2016, CLIN MED BIOCH, V2, P2
[4]   How many rare diseases are there? [J].
Haendel, Melissa ;
Vasilevsky, Nicole ;
Unni, Deepak ;
Bologa, Cristian ;
Harris, Nomi ;
Rehm, Heidi ;
Hamosh, Ada ;
Baynam, Gareth ;
Groza, Tudor ;
McMurry, Julie ;
Dawkins, Hugh ;
Rath, Ana ;
Thaxon, Courtney ;
Bocci, Giovanni ;
Joachimiak, Marcin P. ;
Koehler, Sebastian ;
Robinson, Peter N. ;
Mungall, Chris ;
Oprea, Tudor I. .
NATURE REVIEWS DRUG DISCOVERY, 2020, 19 (02) :77-78
[5]   A call for an integrated approach to improve efficiency, equity and sustainability in rare disease research in the United States [J].
Halley, Meghan C. ;
Smith, Hadley Stevens ;
Ashley, Euan A. ;
Goldenberg, Aaron J. ;
Tabor, Holly K. .
NATURE GENETICS, 2022, 54 (03) :219-222
[6]   Deep Residual Learning for Image Recognition [J].
He, Kaiming ;
Zhang, Xiangyu ;
Ren, Shaoqing ;
Sun, Jian .
2016 IEEE CONFERENCE ON COMPUTER VISION AND PATTERN RECOGNITION (CVPR), 2016, :770-778
[7]   Supportive and symptomatic management of amyotrophic lateral sclerosis [J].
Hobson, Esther V. ;
McDermott, Christopher J. .
NATURE REVIEWS NEUROLOGY, 2016, 12 (09) :526-538
[8]  
Hoskins Amber, 2022, Med Ref Serv Q, V41, P389, DOI 10.1080/02763869.2022.2131143
[9]   eRAM: encyclopedia of rare disease annotations for precision medicine [J].
Jia, Jinmeng ;
An, Zhongxin ;
Ming, Yue ;
Guo, Yongli ;
Li, Wei ;
Liang, Yunxiang ;
Guo, Dongming ;
Li, Xin ;
Tai, Jun ;
Chen, Geng ;
Jin, Yaqiong ;
Liu, Zhimei ;
Ni, Xin ;
Shi, Tieliu .
NUCLEIC ACIDS RESEARCH, 2018, 46 (D1) :D937-D943
[10]  
Kipf T. N., 2016, ICLR, P1