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

vh8:-B5KL92VK-8
  skos:prefLabel "glycogénose de type IV"@fr, "glycogen storage disease type IV"@en ;
  a skos:Concept ;
  skos:broader vh8:-HKHNT5BS-P .

vh8:-G37XWGTK-R
  skos:prefLabel "enzymopathy"@en, "enzymopathie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-HKHNT5BS-P .

vh8: a skos:ConceptScheme .
vh8:-Z6NSSV8H-M
  skos:prefLabel "glycogénose de type I"@fr, "glycogen storage disease type I"@en ;
  a skos:Concept ;
  skos:broader vh8:-HKHNT5BS-P .

vh8:-ZS5BP8PL-6
  skos:prefLabel "glycogen storage disease type V"@en, "glycogénose de type V"@fr ;
  a skos:Concept ;
  skos:broader vh8:-HKHNT5BS-P .

vh8:-RV81R22T-S
  skos:prefLabel "glycogénose de type II"@fr, "glycogen storage disease type II"@en ;
  a skos:Concept ;
  skos:broader vh8:-HKHNT5BS-P .

vh8:-XHP5QC0J-T
  skos:prefLabel "glycogen storage disease type VII"@en, "glycogénose de type VII"@fr ;
  a skos:Concept ;
  skos:broader vh8:-HKHNT5BS-P .

vh8:-D04C2ZLN-X
  skos:prefLabel "glycogénose de type VIII"@fr, "glycogen storage disease type VIII"@en ;
  a skos:Concept ;
  skos:broader vh8:-HKHNT5BS-P .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-HKHNT5BS-P .

vh8:-XG4NPZBJ-T
  skos:prefLabel "glycogen storage disease type III"@en, "glycogénose de type III"@fr ;
  a skos:Concept ;
  skos:broader vh8:-HKHNT5BS-P .

vh8:-H64GCFZV-9
  skos:prefLabel "glycogen storage disease type VI"@en, "glycogénose de type VI"@fr ;
  a skos:Concept ;
  skos:broader vh8:-HKHNT5BS-P .

vh8:-HKHNT5BS-P
  skos:inScheme vh8: ;
  skos:narrower vh8:-B5KL92VK-8, vh8:-XHP5QC0J-T, vh8:-ZS5BP8PL-6, vh8:-D04C2ZLN-X, vh8:-RV81R22T-S, vh8:-Z6NSSV8H-M, vh8:-H64GCFZV-9, vh8:-XG4NPZBJ-T ;
  skos:prefLabel "glycogénose"@fr, "glycogenosis"@en ;
  skos:definition "A glycogen storage disease (GSD, also glycogenosis and dextrinosis) is a metabolic disorder caused by enzyme deficiencies affecting either glycogen synthesis, glycogen breakdown or glycolysis (glucose breakdown), typically within muscles and/or liver cells.GSD has two classes of cause: genetic and acquired. (Wikipedia)"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Glycogen_storage_disease> ;
  skos:broader vh8:-N32K7HZ8-D, vh8:-G37XWGTK-R ;
  a skos:Concept .