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

vh8:-JB5S9971-3
  skos:prefLabel "syndrome de Meckel"@fr, "Meckel syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-Z70D31CR-F .

vh8:-ZW5H18F8-6
  skos:prefLabel "syndrome de Zellweger"@fr, "cerebrohepatorenal syndrome"@en ;
  a skos:Concept ;
  skos:broader vh8:-Z70D31CR-F .

vh8:-Z70D31CR-F
  skos:exactMatch <https://en.wikipedia.org/wiki/Polycystic_kidney_disease>, <https://fr.wikipedia.org/wiki/Polykystose_r%C3%A9nale_type_dominant> ;
  skos:broader vh8:-N32K7HZ8-D, vh8:-FHQ8ZP5D-3, vh8:-M1KXDZ6M-D ;
  skos:narrower vh8:-ZW5H18F8-6, vh8:-JB5S9971-3 ;
  skos:inScheme vh8: ;
  skos:definition "Polycystic kidney disease (PKD or PCKD, also known as polycystic kidney syndrome) is a genetic disorder in which the renal tubules become structurally abnormal, resulting in the development and growth of multiple cysts within the kidney. (Wikipedia)"@en, "La polykystose rénale type dominant (PKD) est la plus fréquente des maladies héréditaires monogéniques du rein. Elle se caractérise par l’apparition lente et progressive de kystes principalement au niveau des reins. (Wikipédia)"@fr ;
  a skos:Concept ;
  skos:prefLabel "rein polykystique"@fr, "polycystic kidney"@en .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-Z70D31CR-F .

vh8:-FHQ8ZP5D-3
  skos:prefLabel "kyste"@fr, "cyst"@en ;
  a skos:Concept ;
  skos:narrower vh8:-Z70D31CR-F .

vh8:-M1KXDZ6M-D
  skos:prefLabel "kidney disease"@en, "pathologie du rein"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-Z70D31CR-F .