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

vh8:-P9GV521K-5
  skos:definition "Le syndrome de Cowden, ou maladie de Cowden, est une rare maladie génétique caractérisé par des hamartomes multiples et disséminés, et par un risque accru de développer certaines tumeurs malignes. (Wikipédia)"@fr, "Cowden syndrome (also known as Cowden's disease and multiple hamartoma syndrome) is an autosomal dominant inherited condition characterized by benign overgrowths called hamartomas as well as an increased lifetime risk of breast, thyroid, uterine, and other cancers. (Wikipedia)"@en ;
  a skos:Concept ;
  skos:prefLabel "Cowden syndrome"@en, "syndrome de Cowden"@fr ;
  skos:broader vh8:-ZCXD6XRV-0, vh8:-N32K7HZ8-D, vh8:-M7X3NL2G-F, vh8:-N5XVRNBC-C ;
  skos:inScheme vh8: ;
  skos:exactMatch <https://en.wikipedia.org/wiki/Cowden_syndrome>, <https://fr.wikipedia.org/wiki/Syndrome_de_Cowden> .

vh8:-N5XVRNBC-C
  skos:prefLabel "tumeur"@fr, "tumor"@en ;
  a skos:Concept ;
  skos:narrower vh8:-P9GV521K-5 .

vh8:-ZCXD6XRV-0
  skos:prefLabel "hamartome"@fr, "hamartoma"@en ;
  a skos:Concept ;
  skos:narrower vh8:-P9GV521K-5 .

vh8: a skos:ConceptScheme .
vh8:-M7X3NL2G-F
  skos:prefLabel "pathologie de la peau"@fr, "skin disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-P9GV521K-5 .

vh8:-N32K7HZ8-D
  skos:prefLabel "hereditary disease"@en, "maladie héréditaire"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-P9GV521K-5 .