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

vh8:-TX6ZBC03-T
  skos:prefLabel "dysmorphie faciale"@fr, "dysmorphic facies"@en ;
  a skos:Concept ;
  skos:narrower vh8:-M3LC26R0-0 .

vh8:-M3LC26R0-0
  skos:broader vh8:-MF2505S3-R, vh8:-TX6ZBC03-T, vh8:-ZTQ66C9Q-S, vh8:-TT4GBZDF-H, vh8:-H9F6VJ33-7, vh8:-GJR46JS3-Z, vh8:-KH3C90B4-7 ;
  skos:prefLabel "syndrome de Patau"@fr, "Patau syndrome"@en ;
  skos:exactMatch <https://fr.wikipedia.org/wiki/Trisomie_13>, <https://www.wikidata.org/wiki/Q284219>, <https://en.wikipedia.org/wiki/Patau_syndrome> ;
  skos:altLabel "trisomy 13"@en, "trisomie 13"@fr ;
  a skos:Concept ;
  skos:inScheme vh8: ;
  skos:definition "Patau syndrome is a syndrome caused by a chromosomal abnormality, in which some or all of the cells of the body contain extra genetic material from chromosome 13. The extra genetic material disrupts normal development, causing multiple and complex organ defects. (Wikipedia)"@en, "La trisomie 13, ou syndrome de Patau, est la pathologie qui résulte de la présence d’un chromosome 13 supplémentaire. (Wikipédia)"@fr .

vh8: a skos:ConceptScheme .
vh8:-GJR46JS3-Z
  skos:prefLabel "trisomy"@en, "trisomie"@fr ;
  a skos:Concept ;
  skos:narrower vh8:-M3LC26R0-0 .

vh8:-ZTQ66C9Q-S
  skos:prefLabel "polydactylie"@fr, "polydactyly"@en ;
  a skos:Concept ;
  skos:narrower vh8:-M3LC26R0-0 .

vh8:-KH3C90B4-7
  skos:prefLabel "cardiopathie congénitale"@fr, "congenital heart disease"@en ;
  a skos:Concept ;
  skos:narrower vh8:-M3LC26R0-0 .

vh8:-MF2505S3-R
  skos:prefLabel "pathologie de l'encéphale"@fr, "cerebral disorder"@en ;
  a skos:Concept ;
  skos:narrower vh8:-M3LC26R0-0 .

vh8:-TT4GBZDF-H
  skos:prefLabel "retard psychomoteur"@fr, "psychomotor retardation"@en ;
  a skos:Concept ;
  skos:narrower vh8:-M3LC26R0-0 .

vh8:-H9F6VJ33-7
  skos:prefLabel "chromosome D13 anormal"@fr, "abnormal chromosome D13"@en ;
  a skos:Concept ;
  skos:narrower vh8:-M3LC26R0-0 .