DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants - Wikidata - wikimedia - TriplyDB

DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants

DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants

http://www.wikidata.org/entity/Q28584435

about

Harnessing public domain data to discover and validate therapeutic targets.Integrative Analysis of Brain Region-specific Shank3 Interactomes for Understanding the Heterogeneity of Neuronal Pathophysiology Related to SHANK3 Mutations.A knowledge-based framework for the discovery of cancer-predisposing variants using large-scale sequencing breast cancer data Distinct DNA methylation profiles in subtypes of orofacial cleft.HGPEC: a Cytoscape app for prediction of novel disease-gene and disease-disease associations and evidence collection based on a random walk on heterogeneous network.Striatal Transcriptome and Interactome Analysis of Shank3-overexpressing Mice Reveals the Connectivity between Shank3 and mTORC1 Signaling.Open Targets: a platform for therapeutic target identification and validation WebGestalt 2017: a more comprehensive, powerful, flexible and interactive gene set enrichment analysis toolkit.eDGAR: a database of Disease-Gene Associations with annotated Relationships among genes Domain-based prediction of the human isoform interactome provides insights into the functional impact of alternative splicing.Machine Learning-Based Gene Prioritization Identifies Novel Candidate Risk Genes for Inflammatory Bowel Disease.Reverse Nearest Neighbor Search on a Protein-Protein Interaction Network to Infer Protein-Disease Associations Network-based Approaches in Pharmacology.Cross-Kingdom Regulation of Putative miRNAs Derived from Happy Tree in Cancer Pathway: A Systems Biology Approach.Extracellular vesicle-packaged miRNA release after short-term exposure to particulate matter is associated with increased coagulation.Reliable Granular References to Changing Linked Data Systematic integration of biomedical knowledge prioritizes drugs for repurposing.Orthologue chemical space and its influence on target prediction.DISNOR: a disease network open resource.A deep ensemble model to predict miRNA-disease association.Estimation of the proteomic cancer co-expression sub networks by using association estimators.eRAM: encyclopedia of rare disease annotations for precision medicine.TissGDB: tissue-specific gene database in cancer.Unsupervised gene expression analyses identify IPF-severity correlated signatures, associated genes and biomarkers.PedAM: a database for Pediatric Disease Annotation and Medicine.Genome variation and conserved regulation identify genomic regions responsible for strain specific phenotypes in rat.The online Tabloid Proteome: an annotated database of protein associations.Text mining and expert curation to develop a database on psychiatric diseases and their genes.A census of P. longum's phytochemicals and their network pharmacological evaluation for identifying novel drug-like molecules against various diseases, with a special focus on neurological disorders.Personal Cancer Genome Reporter: variant interpretation report for precision oncology.The integration of weighted gene association networks based on information entropy.tmVar 2.0: integrating genomic variant information from literature with dbSNP and ClinVar for precision medicine.psygenet2r: a R/Bioconductor package for the analysis of psychiatric disease genes.Properties of human genes guided by their enrichment in rare and common variants.Query expansion using MeSH terms for dataset retrieval: OHSU at the bioCADDIE 2016 dataset retrieval challenge.A systems biology analysis protein-protein interaction of NASH and IBD based on comprehensive gene information.An integrative functional genomics framework for effective identification of novel regulatory variants in genome-phenome studies.Sulfonanilide Derivatives in Identifying Novel Aromatase Inhibitors by Applying Docking, Virtual Screening, and MD Simulations Studies.Lnc2Catlas: an atlas of long noncoding RNAs associated with risk of cancers.MiRNA-mRNA crosstalk in laryngeal squamous cell carcinoma based on the TCGA database.

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DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants

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2017 nî lūn-bûn

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Alba Gutiérrez-Sacristán

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Emilio Centeno

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Javier García-García

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

A computational framework to infer human disease-associated long noncoding RNAs

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 Human Phenotype Ontology: Semantic Unification of Common and Rare Disease

Disease Ontology 2015 update: an expanded and updated database of human diseases for linking biomedical knowledge through disease data

WikiPathways: capturing the full diversity of pathway knowledge

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

dbSNP: the NCBI database of genetic variation

A global reference for human genetic variation

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Núria Queralt Rosinach

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