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

Individualized Medicine from Prewomb to Tomb

(2014) Eric J. Topol   CELL

Multiple evidence strands suggest that there may be as few as 19 000 human protein-coding genes

(2014) Iakes Ezkurdia et al.   HUMAN MOLECULAR GENETICS

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

(2014) Michel Dumontier et al.   Journal of Biomedical Semantics

The Rat Genome Database 2013--data, tools and users

(2013) S. J. F. Laulederkind et al.   BRIEFINGS IN BIOINFORMATICS

An innovative portal for rare genetic diseases research: The semantic Diseasecard

(2013) Pedro Lopes et al.   JOURNAL OF BIOMEDICAL INFORMATICS

The Mouse Genome Database: integration of and access to knowledge about the laboratory mouse

(2013) Judith A. Blake et al.   NUCLEIC ACIDS RESEARCH

Activities at the Universal Protein Resource (UniProt)

(2013)   NUCLEIC ACIDS RESEARCH

The Human Phenotype Ontology project: linking molecular biology and disease through phenotype data

(2013) Sebastian Köhler et al.   NUCLEIC ACIDS RESEARCH

The Reactome pathway knowledgebase

(2013) David Croft et al.   NUCLEIC ACIDS RESEARCH

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

(2013) Danielle Welter et al.   NUCLEIC ACIDS RESEARCH

NCBI’s Database of Genotypes and Phenotypes: dbGaP

(2013) Kimberly A. Tryka et al.   NUCLEIC ACIDS RESEARCH

MalaCards: an integrated compendium for diseases and their annotation

(2013) Noa Rappaport et al.   Database-The Journal of Biological Databases and Curation

Semantic Web meets Integrative Biology: a survey

(2012) H. Chen et al.   BRIEFINGS IN BIOINFORMATICS

The EU-ADR corpus: Annotated drugs, diseases, targets, and their relationships

(2012) Erik M. van Mulligen et al.   JOURNAL OF BIOMEDICAL INFORMATICS

The Comparative Toxicogenomics Database: update 2013

(2012) Allan Peter Davis et al.   NUCLEIC ACIDS RESEARCH

Introduction to Translational Bioinformatics Collection

(2012) Russ B. Altman   PLoS Computational Biology

Translational bioinformatics: linking knowledge across biological and clinical realms: Figure 1

(2011) Indra Neil Sarkar et al.   JOURNAL OF THE AMERICAN MEDICAL INFORMATICS ASSOCIATION

Disease Ontology: a backbone for disease semantic integration

(2011) L. M. Schriml et al.   NUCLEIC ACIDS RESEARCH

Gene-Disease Network Analysis Reveals Functional Modules in Mendelian, Complex and Environmental Diseases

(2011) Anna Bauer-Mehren et al.   PLoS One

DisGeNET: a Cytoscape plugin to visualize, integrate, search and analyze gene–disease networks

(2010) Anna Bauer-Mehren et al.   BIOINFORMATICS

Single nucleotide polymorphisms in obesity-related genes and all-cause and cause-specific mortality: a prospective cohort study

(2009) Lisa Gallicchio et al.   BMC Medical Genetics

Gender-specific effect of Pro12Ala polymorphism in peroxisome proliferator-activated receptor γ-2 gene on obesity risk and leptin levels in a Tunisian population

(2009) Samir Ben Ali et al.   CLINICAL BIOCHEMISTRY

PANTHER version 7: improved phylogenetic trees, orthologs and collaboration with the Gene Ontology Consortium

(2009) Huaiyu Mi et al.   NUCLEIC ACIDS RESEARCH

Atp7b−/−mice as a model for studies of Wilson's disease

(2008) Svetlana Lutsenko   BIOCHEMICAL SOCIETY TRANSACTIONS

Extraction of semantic biomedical relations from text using conditional random fields

(2008) Markus Bundschus et al.   BMC BIOINFORMATICS

The genetic susceptibility to type 2 diabetes may be modulated by obesity status: implications for association studies

(2008) Stéphane Cauchi et al.   BMC Medical Genetics

Bio2RDF: Towards a mashup to build bioinformatics knowledge systems

(2008) François Belleau et al.   JOURNAL OF BIOMEDICAL INFORMATICS

McKusick's Online Mendelian Inheritance in Man (OMIM(R))

(2008) J. Amberger et al.   NUCLEIC ACIDS RESEARCH