Discovery of disease- and drug-specific pathways through community structures of a literature network
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Olivier Lichtarge | Stephen J. Wilson | Harikumar Govindarajan | Chih-Hsu Lin | Minh Pham | Stephen Wilson | O. Lichtarge | Harikumar Govindarajan | Chih-Hsu Lin | Minh Pham
[1] Núria Queralt-Rosinach,et al. DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants , 2016, Nucleic Acids Res..
[2] Thomas C. Rindflesch,et al. Large-Scale Structure of a Network of Co-Occurring MeSH Terms: Statistical Analysis of Macroscopic Properties , 2014, PloS one.
[3] Prudence Mutowo-Meullenet,et al. The GOA database: Gene Ontology annotation updates for 2015 , 2014, Nucleic Acids Res..
[4] Alan F. Scott,et al. Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders , 2002, Nucleic Acids Res..
[5] Chris T. A. Evelo,et al. WikiPathways: building research communities on biological pathways , 2011, Nucleic Acids Res..
[6] Helga Thorvaldsdóttir,et al. Molecular signatures database (MSigDB) 3.0 , 2011, Bioinform..
[7] Hsuan-Cheng Huang,et al. Dissecting the Human Protein-Protein Interaction Network via Phylogenetic Decomposition , 2014, Scientific Reports.
[8] Krin A. Kay,et al. The implications of human metabolic network topology for disease comorbidity , 2008, Proceedings of the National Academy of Sciences.
[9] Peer Bork,et al. The SIDER database of drugs and side effects , 2015, Nucleic Acids Res..
[10] Sophia Ananiadou,et al. FACTA: a text search engine for finding associated biomedical concepts , 2008, Bioinform..
[11] Henning Hermjakob,et al. The Reactome pathway knowledgebase , 2013, Nucleic Acids Res..
[12] K. E. Ravikumar,et al. A Biological Named Entity Recognizer , 2002, Pacific Symposium on Biocomputing.
[13] Andrew D. Rouillard,et al. Enrichr: a comprehensive gene set enrichment analysis web server 2016 update , 2016, Nucleic Acids Res..
[14] Joyce A. Mitchell,et al. Using literature-based discovery to identify disease candidate genes , 2005, Int. J. Medical Informatics.
[15] J. Nelson,et al. Augmentation treatment in major depressive disorder: focus on aripiprazole , 2008, Neuropsychiatric disease and treatment.
[16] Maryam Habibi,et al. Deep learning with word embeddings improves biomedical named entity recognition , 2017, Bioinform..
[17] Davide Heller,et al. STRING v10: protein–protein interaction networks, integrated over the tree of life , 2014, Nucleic Acids Res..
[18] Hiroyuki Ogata,et al. KEGG: Kyoto Encyclopedia of Genes and Genomes , 1999, Nucleic Acids Res..
[19] Jean-Loup Guillaume,et al. Fast unfolding of communities in large networks , 2008, 0803.0476.
[20] Charles F. Bearden,et al. A Nondegenerate Code of Deleterious Variants in Mendelian Loci Contributes to Complex Disease Risk , 2013, Cell.
[21] The Gene Ontology Consortium,et al. Expansion of the Gene Ontology knowledgebase and resources , 2016, Nucleic Acids Res..
[22] Jari Björne,et al. Large-Scale Event Extraction from Literature with Multi-Level Gene Normalization , 2013, PloS one.
[23] Thomas C. Wiegers,et al. A CTD–Pfizer collaboration: manual curation of 88 000 scientific articles text mined for drug–disease and drug–phenotype interactions , 2013, Database J. Biol. Databases Curation.
[24] The Gene Ontology Consortium. Expansion of the Gene Ontology knowledgebase and resources , 2016, Nucleic Acids Res..
[25] Damian Szklarczyk,et al. STITCH 5: augmenting protein–chemical interaction networks with tissue and affinity data , 2015, Nucleic Acids Res..
[26] Angela D. Wilkins,et al. Discovery of Functional and Disease Pathways by Community Detection in Protein-Protein Interaction Networks , 2017, PSB.
[27] Núria Queralt-Rosinach,et al. Extraction of relations between genes and diseases from text and large-scale data analysis: implications for translational research , 2014, BMC Bioinformatics.
[28] Angela D. Wilkins,et al. Automated literature mining and hypothesis generation through a network of Medical Subject Headings , 2018, bioRxiv.
[29] Dietrich Rebholz-Schuhmann,et al. EBIMed - text crunching to gather facts for proteins from Medline , 2007, Bioinform..
[30] Damian Szklarczyk,et al. STRING v9.1: protein-protein interaction networks, with increased coverage and integration , 2012, Nucleic Acids Res..
[31] Jure Leskovec,et al. Overlapping community detection at scale: a nonnegative matrix factorization approach , 2013, WSDM.
[32] Deanna M. Church,et al. ClinVar: public archive of relationships among sequence variation and human phenotype , 2013, Nucleic Acids Res..
[33] Robert Leaman,et al. PubTator central: automated concept annotation for biomedical full text articles , 2019, Nucleic Acids Res..
[34] J. Mesirov,et al. The Molecular Signatures Database Hallmark Gene Set Collection , 2015 .
[35] Gang Feng,et al. Disease Ontology: a backbone for disease semantic integration , 2011, Nucleic Acids Res..
[36] M. Newman,et al. Finding community structure in very large networks. , 2004, Physical review. E, Statistical, nonlinear, and soft matter physics.
[37] Sampo Pyysalo,et al. Overview of the Cancer Genetics and Pathway Curation tasks of BioNLP Shared Task 2013 , 2015, BMC Bioinformatics.
[38] Angela N. Brooks,et al. A Next Generation Connectivity Map: L1000 Platform And The First 1,000,000 Profiles , 2017 .
[39] Shang-Hua Teng,et al. Finding local communities in protein networks , 2009, BMC Bioinformatics.
[40] Fei Li,et al. A neural joint model for entity and relation extraction from biomedical text , 2017, BMC Bioinformatics.
[41] Rob Jelier,et al. CoPub Mapper: mining MEDLINE based on search term co-publication , 2005, BMC Bioinformatics.
[42] Alfonso Valencia,et al. Text-mining approaches in molecular biology and biomedicine. , 2005, Drug discovery today.
[43] Thomas C. Wiegers,et al. The Comparative Toxicogenomics Database: update 2019 , 2018, Nucleic Acids Res..