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

vh8:-GBVG8KXN-6
  skos:prefLabel "kyste branchial"@fr, "branchial cyst"@en ;
  a skos:Concept ;
  skos:narrower vh8:-ZZ603TW5-M .

vh8:-QNVGZ5NQ-W
  skos:prefLabel "renal dysplasia"@en, "dysplasie rénale"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-ZZ603TW5-M .

vh8:-ZZ603TW5-M
  skos:broader vh8:-C2PD3NRH-2, vh8:-N32K7HZ8-D, vh8:-QG1RVCT9-L, vh8:-QNVGZ5NQ-W, vh8:-GBVG8KXN-6 ;
  skos:altLabel "branchio-oto-renal syndrome"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Branchio-oto-renal_syndrome> ;
  skos:prefLabel "syndrome de Melnick-Fraser"@fr, "Melnick-Fraser syndrome"@en ;
  a skos:Concept ;
  skos:definition "Branchio-oto-renal syndrome (BOR) , is an autosomal dominant genetic disorder involving the kidneys, ears, and neck. (Wikipedia)"@en ;
  skos:inScheme vh8: .

vh8:-C2PD3NRH-2
  skos:prefLabel "hearing loss"@en, "surdité"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-ZZ603TW5-M .

vh8: a skos:ConceptScheme .
vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-ZZ603TW5-M .

vh8:-QG1RVCT9-L
  skos:prefLabel "complex syndrome"@en, "syndrome complexe"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-ZZ603TW5-M .