@prefix dcat:    <https://www.w3.org/ns/dcat#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix foaf:    <http://xmlns.com/foaf/0.1/> .
@prefix xsd:     <http://www.w3.org/2001/XMLSchema#> .
@prefix ordo:    <http://www.orpha.net/ORDO/Orphanet_> .
@prefix omim:    <https://omim.org/entry/> .
@prefix hp:      <http://purl.obolibrary.org/obo/HP_> .
@prefix mondo:   <http://purl.obolibrary.org/obo/MONDO_> .
@prefix prov:    <http://www.w3.org/ns/prov#> .
@prefix schema:  <https://schema.org/> .


# Flat community submissions index
# Auto-generated 2026-04-12 | 2 case(s)
# Source: https://github.com/StaticFDP/ga4gh-rare-disease-trajectories/issues?q=label%3Adisease-case

<https://fdp.semscape.org/ga4gh-rare-disease-trajectories/fdp/submissions/2> a dcat:Dataset ;
    dcterms:title "Duchenne muscular dystrophy (DMD)"@en ;
    dcterms:description "The Duchenne Data Platform (DDP) aggregates longitudinal patient data for Duchenne muscular dystrophy across European patient communities. The platform captures clinical measurements (6-minute walk test, North Star Ambulatory Assessment, pulmonary function tests), genetic data (exon deletions, point mutations, duplications), and treatment history (corticosteroids, exon skipping therapies, gene therapy trials). Disease trajectory modeling focuses on ambulatory to non-ambulatory transition and car"@en ;
    dcterms:created "2026-04-12"^^xsd:date ;
    dcat:landingPage <https://github.com/StaticFDP/ga4gh-rare-disease-trajectories/issues/2> ;
    dcterms:subject <http://www.orpha.net/ORDO/Orphanet_98895> ;
    dcterms:subject <https://omim.org/entry/310200> ;
    dcterms:subject <http://purl.obolibrary.org/obo/MONDO_0010679> ;
    dcat:keyword "Duchenne Data Platform (Duchenne Parent Project / FAIR Data Systems S.L.)"@en ;
    dcterms:creator [ foaf:name "Duchenne Parent Project — World Duchenne Organization" ] .

<https://fdp.semscape.org/ga4gh-rare-disease-trajectories/fdp/submissions/1> a dcat:Dataset ;
    dcterms:title "Amyotrophic lateral sclerosis (ALS)"@en ;
    dcterms:description "ALS TDI maintains a comprehensive patient registry tracking disease trajectory for ALS patients. The registry captures longitudinal phenotype data including motor function decline, respiratory measures, and survival outcomes. Data is structured using HPO terms and mapped to Phenopackets v2 format. The disease trajectory spans from initial symptom onset through progression stages, with particular focus on identifying biomarkers of disease progression rate and therapeutic response."@en ;
    dcterms:created "2026-04-12"^^xsd:date ;
    dcat:landingPage <https://github.com/StaticFDP/ga4gh-rare-disease-trajectories/issues/1> ;
    dcterms:subject <http://www.orpha.net/ORDO/Orphanet_803> ;
    dcterms:subject <https://omim.org/entry/105400> ;
    dcterms:subject <http://purl.obolibrary.org/obo/MONDO_0004976> ;
    dcat:keyword "ALS TDI Registry (ALS Therapy Development Institute)"@en ;
    dcterms:creator [ foaf:name "ALS TDI Data Team" ] .