Raras is an open, FAIR-compliant knowledge graph of rare diseases — the largest in Latin America — integrating Orphanet, the Human Phenotype Ontology (HPO), OMIM, MONDO, ClinVar, Open Targets, PubMed and ClinicalTrials.gov with Brazilian public-health (SUS) data. It mints stable RARAS identifiers for diseases, reference centers, protocols, associations, communities and medications, each resolvable as Linked Data (SPARQL, RDF, GraphQL, GA4GH Beacon/Phenopackets) with a dereferenceable vocabulary and VOID/DCAT metadata.
Identifiers resolve via content negotiation (303 to HTML, Turtle/JSON-LD for machines) at https://raras.org/id/$1 — e.g. https://raras.org/id/D00166. The vocabulary is published at https://raras.org/ontology and dataset metadata at https://raras.org/.well-known/void (VOID + DCAT). SPARQL 1.1 endpoint: https://raras.org/api/sparql. Group contact email: hello@raras.org
raras
Local identifiers in Raras Brazilian Rare Disease Knowledge Graph should match this
regular expression:
^[DCPAGMST]\d{5,6}$
Compact URIs (CURIEs) constructed from Raras Brazilian Rare Disease Knowledge Graph should match
this regular expression:
^raras:[DCPAGMST]\d{5,6}$
A provider turns a local unique identifiers from a resource into a URI. Many providers are also resolvable as URLs (i.e., they can be used in a web browser).
The local unique identifier D00166 is used to demonstrate the providers
available for Raras Brazilian Rare Disease Knowledge Graph. Some providers may use a different example, which is displayed in the table below.
A guide for curating additional providers can be found
here.
| Provider Name | Provider Code | URI |
|---|---|---|
| Raras Brazilian Rare Disease Knowledge Graph | raras |
https://raras.org/id/D00166 |
| Raras Brazilian Rare Disease Knowledge Graph (RDF) | rdf |
https://raras.org/id/D00166 |
| Bioregistry | bioregistry |
https://bioregistry.io/raras:D00166 |