DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes - Wikidata - wikimedia - TriplyDB

DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes

DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes

http://www.wikidata.org/entity/Q28649649

about

PsyGeNET: a knowledge platform on psychiatric disorders and their genes WikiPathways: capturing the full diversity of pathway knowledge Using the Semantic Web for Rapid Integration of WikiPathways with Other Biological Online Data Resources.Using Multi-objective Optimization to Identify Dynamical Network Biomarkers as Early-warning Signals of Complex Diseases.DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants POSTAR: a platform for exploring post-transcriptional regulation coordinated by RNA-binding proteins MalaCards: an amalgamated human disease compendium with diverse clinical and genetic annotation and structured search DisGeNET-RDF: harnessing the innovative power of the Semantic Web to explore the genetic basis of diseases Profiling RNA editing in human tissues: towards the inosinome Atlas mutLBSgeneDB: mutated ligand binding site gene DataBase.Drug repurposing from the perspective of pharmaceutical companies.Literature evidence in open targets - a target validation platform Genome-wide analysis of differential RNA editing in epilepsy.A network-based method for mechanistic investigation of Shexiang Baoxin Pill's treatment of cardiovascular diseases.Allele, phenotype and disease data at Mouse Genome Informatics: improving access and analysis In Search of 'Birth Month Genes': Using Existing Data Repositories to Locate Genes Underlying Birth Month-Disease Relationships.Fusing literature and full network data improves disease similarity computation.FocusHeuristics - expression-data-driven network optimization and disease gene prediction Open PHACTS computational protocols for in silico target validation of cellular phenotypic screens: knowing the knowns.Learning from biomedical linked data to suggest valid pharmacogenes.Human fetal heart specific coexpression network involves congenital heart disease/defect candidate genes.Recent advances in predicting gene-disease associations GLADIATOR: a global approach for elucidating disease modules.Accurately annotate compound effects of genetic variants using a context-sensitive framework.Integrative information theoretic network analysis for genome-wide association study of aspirin exacerbated respiratory disease in Korean population.Striatal Transcriptome and Interactome Analysis of Shank3-overexpressing Mice Reveals the Connectivity between Shank3 and mTORC1 Signaling.Comorbidities in the diseasome are more apparent than real: What Bayesian filtering reveals about the comorbidities of depression Genome-Wide Linkage Analysis of Large Multiple Multigenerational Families Identifies Novel Genetic Loci for Coronary Artery Disease.Architecture of the human interactome defines protein communities and disease networks.A pipeline for the systematic identification of non-redundant full-ORF cDNAs for polymorphic and evolutionary divergent genomes: Application to the ascidian Ciona intestinalis.A Continuous Correlated Beta Process Model for Genetic Ancestry in Admixed Populations DNetDB: The human disease network database based on dysfunctional regulation mechanism The Network Library: a framework to rapidly integrate network biology resources.A functional module-based exploration between inflammation and cancer in esophagus.QueryOR: a comprehensive web platform for genetic variant analysis and prioritization PCOSKB: A KnowledgeBase on genes, diseases, ontology terms and biochemical pathways associated with PolyCystic Ovary Syndrome.Revealing potential molecular targets bridging colitis and colorectal cancer based on multidimensional integration strategy.Uncovering disease mechanisms through network biology in the era of Next Generation Sequencing.Building a glaucoma interaction network using a text mining approach.Purifying selection shapes the coincident SNP distribution of primate coding sequences.

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DisGeNET: a discovery platform for the dynamical exploration of human diseases and their genes

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Anna Bauer-Mehren

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Jordi Deu-Pons

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Martin Baron

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The Semanticscience Integrated Ontology (SIO) for biomedical research and knowledge discovery

Gene-disease network analysis reveals functional modules in mendelian, complex and environmental diseases

Network medicine analysis of COPD multimorbidities

Extraction of relations between genes and diseases from text and large-scale data analysis: implications for translational research

The Wilson disease gene is a copper transporting ATPase with homology to the Menkes disease gene

Gene indexing: characterization and analysis of NLM's GeneRIFs

The Reactome pathway knowledgebase

The NHGRI GWAS Catalog, a curated resource of SNP-trait associations

The NCBI dbGaP database of genotypes and phenotypes

MalaCards: an integrated compendium for diseases and their annotation

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2015

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Núria Queralt Rosinach

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275026545

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