CTD is a robust, publicly available database that aims to advance understanding about how environmental exposures affect human health

STRING is a database of known and predicted protein-protein interactions.

results from studies that have investigated the interaction of genotype and phenotype in humans

The Single Nucleotide Polymorphism Database

PubMed Central® (PMC) is a free full-text archive of biomedical and life sciences journal literature at the U.S. National Institutes of Health's National Library of Medicine (NIH/NLM)

ClinVar aggregates information about genomic variation and its relationship to human health.

The Pharmacogenomics Knowledge Base

The Gene Ontology (GO) knowledgebase is the world’s largest source of information on the functions of genes

Relational data format for Chebi - Dictionary of molecular entities from products of nature or synthetic products used to intervene in the processes of living organisms, incorporating an ontological classification

ClinicalTrials.gov is a database of privately and publicly funded clinical studies conducted around the world.

miRBase: the microRNA database

The 1000 Genomes Project created a catalogue of common human genetic variation, using openly consented samples from people who declared themselves to be healthy.

The Cancer Dependency Map

2.7M data points for 1.2M compounds and 9K targets

A rich and highly specific standardised medical terminology to facilitate sharing of regulatory information internationally for medical products used by humans

An example brick for testing purposes

The NCI's Genomic Data Commons (GDC)

The Genotype-Tissue Expression (GTEx) project is an ongoing effort to build a comprehensive public resource to study tissue-specific gene expression and regulation.

Encyclopedia of genes and genes variants

Organizes information related to human medical genetics, such as attributes of conditions with a genetic contribution.