@prefix n9j: <http://data.loterre.fr/ark:/67375/N9J> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .
@prefix isothes: <http://purl.org/iso25964/skos-thes#> .

n9j:-NN485M62-1
  skos:prefLabel "chromosome disorders"@en ;
  a skos:Concept ;
  skos:narrower n9j:-NRRK4WF1-4 .

n9j:-NRRK4WF1-4
  skos:broader n9j:-JDKM608R-K, n9j:-QTWNL3VC-C, n9j:-V2N6B3MZ-7, n9j:-G8G21TPB-D, n9j:-ZSNHB585-F, n9j:-NN485M62-1, n9j:-VMT0H494-3 ;
  skos:definition "Prader-Willi syndrome (PWS) is a rare, inherited chromosomal disorder arising from deletion or disruption of genes in the proximal arm of chromosome 15. It was first described in 1956 by Andrea Prader, Heinrich Willi, Alexis Labhart, Andrew Ziegler, and Guido Fanconi of Switzerland. [Source: Encyclopedia of Global Health; Prader-Willi Syndrome]"@en ;
  a skos:Concept ;
  owl:sameAs <https://concepts.sagepub.com/social-science/concept/Prader-Willi_syndrome> ;
  skos:inScheme n9j: ;
  skos:prefLabel "Prader-Willi syndrome"@en ;
  skos:exactMatch <https://id.nlm.nih.gov/mesh/D011218.html> .

n9j:-V2N6B3MZ-7
  skos:prefLabel "systemic diseases"@en ;
  a skos:Concept ;
  skos:narrower n9j:-NRRK4WF1-4 .

n9j: a skos:ConceptScheme .
n9j:-QTWNL3VC-C
  skos:prefLabel "biological or genetic contributors to obesity"@en ;
  a skos:Concept ;
  skos:narrower n9j:-NRRK4WF1-4 .

n9j:-ZSNHB585-F
  skos:prefLabel "intellectual disability"@en ;
  a skos:Concept ;
  skos:narrower n9j:-NRRK4WF1-4 .

n9j:-G8G21TPB-D
  skos:prefLabel "obesity"@en ;
  a skos:Concept ;
  skos:narrower n9j:-NRRK4WF1-4 .

n9j:-VMT0H494-3
  skos:prefLabel "chromosome abnormalities"@en ;
  a skos:Concept ;
  skos:narrower n9j:-NRRK4WF1-4 .

n9j:-JDKM608R-K
  skos:prefLabel "medical conditions"@en ;
  a skos:Concept ;
  skos:narrower n9j:-NRRK4WF1-4 .

n9j:-concepts
  a isothes:ConceptGroup ;
  skos:prefLabel "concepts"@en ;
  skos:member n9j:-NRRK4WF1-4 .