@prefix vh8: <http://data.loterre.fr/ark:/67375/VH8> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .

vh8:-XJF8R7NT-X
  skos:prefLabel "glomerulonephritis"@en, "néphropathie glomérulaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-T6WMQ6XX-B .

vh8:-C2PD3NRH-2
  skos:prefLabel "hearing loss"@en, "surdité"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-T6WMQ6XX-B .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-T6WMQ6XX-B .

vh8:-T6WMQ6XX-B
  skos:definition "Alport syndrome is a genetic disorder affecting around 1 in 5,000-10,000 children, characterized by glomerulonephritis, end-stage kidney disease, and hearing loss. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:broader vh8:-C2PD3NRH-2, vh8:-XJF8R7NT-X, vh8:-N32K7HZ8-D ;
  skos:prefLabel "syndrome d'Alport"@fr, "Alport syndrome"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Alport_syndrome> .