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

ins:-Q90DGQ2Q-0
  skos:prefLabel "mucoviscidose"@fr, "cystic fibrosis"@en ;
  a skos:Concept ;
  skos:broader ins:-MJ2LK90Z-N .

ins:-TTB9NTM9-V
  skos:prefLabel "mitochondrial disease"@en, "cytopathie mitochondriale"@fr ;
  a skos:Concept ;
  skos:broader ins:-MJ2LK90Z-N .

ins:-WGZ3H3FJ-J
  skos:prefLabel "dystrophie musculaire"@fr, "muscular dystrophy"@en ;
  a skos:Concept ;
  skos:broader ins:-MJ2LK90Z-N .

ins:-PRWZ3W8L-C
  skos:prefLabel "maladie génétique"@fr, "genetic disease"@en ;
  a skos:Concept ;
  skos:narrower ins:-MJ2LK90Z-N .

ins:-MJ2LK90Z-N
  skos:exactMatch vh8:-N32K7HZ8-D ;
  skos:broader ins:-PRWZ3W8L-C ;
  skos:prefLabel "maladie héréditaire"@fr, "hereditary disease"@en ;
  skos:narrower ins:-TTB9NTM9-V, ins:-NGCR9NGQ-D, ins:-VTV8M3RD-J, ins:-V1CZRZTR-H, ins:-MRX86TV2-M, ins:-FTF7TMTV-2, ins:-D8FL6L0V-5, ins:-Q90DGQ2Q-0, ins:-WGZ3H3FJ-J ;
  skos:inScheme ins: ;
  a skos:Concept .

ins:-NGCR9NGQ-D
  skos:prefLabel "sickle cell anemia"@en, "anémie à hématies falciformes"@fr ;
  a skos:Concept ;
  skos:broader ins:-MJ2LK90Z-N .

ins:-MRX86TV2-M
  skos:prefLabel "osteogenesis imperfecta"@en, "ostéogenèse imparfaite"@fr ;
  a skos:Concept ;
  skos:broader ins:-MJ2LK90Z-N .

ins:-D8FL6L0V-5
  skos:prefLabel "porphyrie"@fr, "porphyria"@en ;
  a skos:Concept ;
  skos:broader ins:-MJ2LK90Z-N .

ins:-FTF7TMTV-2
  skos:prefLabel "ataxie spinocérébelleuse"@fr, "spinocerebellar ataxia"@en ;
  a skos:Concept ;
  skos:broader ins:-MJ2LK90Z-N .

ins:-VTV8M3RD-J
  skos:prefLabel "hereditary spastic paraplegia"@en, "paraplégie spasmodique héréditaire de Strümpell-Lorrain"@fr ;
  a skos:Concept ;
  skos:broader ins:-MJ2LK90Z-N .

ins:-V1CZRZTR-H
  skos:prefLabel "achondroplasia"@en, "achondroplasie"@fr ;
  a skos:Concept ;
  skos:broader ins:-MJ2LK90Z-N .

ins: a skos:ConceptScheme .