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

n9j: a skos:ConceptScheme .
n9j:-WNXBJ8QP-C
  skos:prefLabel "genetics/genetic testing"@en ;
  a skos:Concept ;
  skos:narrower n9j:-LGDLB4SZ-X .

n9j:-DCZG4RFK-Q
  skos:prefLabel "X-linked intellectual disability"@en ;
  a skos:Concept ;
  skos:narrower n9j:-LGDLB4SZ-X .

n9j:-W3P23HCH-J
  skos:prefLabel "sex chromosome disorders"@en ;
  a skos:Concept ;
  skos:narrower n9j:-LGDLB4SZ-X .

n9j:-VMT0H494-3
  skos:prefLabel "chromosome abnormalities"@en ;
  a skos:Concept ;
  skos:narrower n9j:-LGDLB4SZ-X .

n9j:-JDKM608R-K
  skos:prefLabel "medical conditions"@en ;
  a skos:Concept ;
  skos:narrower n9j:-LGDLB4SZ-X .

n9j:-concepts
  a isothes:ConceptGroup ;
  skos:prefLabel "concepts"@en ;
  skos:member n9j:-LGDLB4SZ-X .

n9j:-LGDLB4SZ-X
  skos:broader n9j:-WNXBJ8QP-C, n9j:-DCZG4RFK-Q, n9j:-W3P23HCH-J, n9j:-JDKM608R-K, n9j:-VMT0H494-3 ;
  skos:exactMatch <https://id.nlm.nih.gov/mesh/D005600.html> ;
  owl:sameAs <https://concepts.sagepub.com/social-science/concept/Fragile_X_syndrome> ;
  skos:definition "Fragile X syndrome (FXS) is the leading cause of inherited mental retardation. It is caused by a change (mutation) in the fragile X mental retardation 1 (FMR1) gene located near the end of the X chromosome. [Source: Encyclopedia of Human Development; Fragile X Syndrome]"@en ;
  a skos:Concept ;
  skos:inScheme n9j: ;
  skos:prefLabel "Fragile X syndrome"@en .