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

vh8:-W8VLNQPS-G
  skos:prefLabel "Wilms tumor"@en, "tumeur de Wilms"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-TPD4G5NK-H .

vh8:-TPD4G5NK-H
  a skos:Concept ;
  skos:broader vh8:-FW0B41GQ-K, vh8:-JW4BV3J7-L, vh8:-TSXZX7B1-R, vh8:-W8VLNQPS-G, vh8:-QJMQSH2H-3 ;
  skos:prefLabel "syndrome WAGR"@fr, "WAGR syndrome"@en ;
  skos:definition "WAGR syndrome (also known as WAGR complex, Wilms tumour-aniridia syndrome, aniridia-Wilms tumour syndrome) is a rare genetic syndrome in which affected children are predisposed to develop Wilms tumour (a tumour of the kidneys), Aniridia (absence of the coloured part of the eye, the iris), Genitourinary anomalies, and mental Retardation. (Wikipedia)"@en ;
  skos:exactMatch <https://en.wikipedia.org/wiki/WAGR_syndrome> ;
  skos:inScheme vh8: .

vh8: a skos:ConceptScheme .
vh8:-FW0B41GQ-K
  skos:prefLabel "aniridia"@en, "aniridie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-TPD4G5NK-H .

vh8:-TSXZX7B1-R
  skos:prefLabel "chromosome C11 anormal"@fr, "abnormal chromosome C11"@en ;
  a skos:Concept ;
  skos:narrower vh8:-TPD4G5NK-H .

vh8:-QJMQSH2H-3
  skos:prefLabel "genital diseases"@en, "pathologie de l'appareil génital"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-TPD4G5NK-H .

vh8:-JW4BV3J7-L
  skos:prefLabel "arriération mentale"@fr, "mental retardation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-TPD4G5NK-H .