@prefix jvr: <http://data.loterre.fr/ark:/67375/JVR> .
@prefix skos: <http://www.w3.org/2004/02/skos/core#> .
@prefix mesh: <http://id.nlm.nih.gov/mesh/vocab#> .
@prefix dc: <http://purl.org/dc/terms/> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix owl: <http://www.w3.org/2002/07/owl#> .

jvr:-WWJHCQRB-K
  skos:prefLabel "surgery (Qualifier)"@en, "chirurgie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-SDXQ5280-F
  skos:prefLabel "mortality (Qualifier)"@en, "mortalité (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-MZSM0WD8-T
  skos:prefLabel "Gènes liés au chromosome X"@fr, "Genes, X-Linked"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-BL0Q8DS8-X .

jvr:-HPKB70N8-W
  skos:prefLabel "rehabilitation (Qualifier)"@en, "rééducation et réadaptation (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-QGXF7H6W-Z
  skos:prefLabel "Glycogen Storage Disease Type VIII"@en, "Glycogénose de type VIII"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-VG20R78F-K
  skos:prefLabel "embryologie (Qualificatif)"@fr, "embryology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-NNF6WD0C-X
  skos:prefLabel "Aicardi Syndrome"@en, "Syndrome d'Aicardi"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-Z9TSGBXH-4
  skos:prefLabel "génétique (Qualificatif)"@fr, "genetics (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-L6C0XPHT-4
  skos:prefLabel "métabolisme (Qualificatif)"@fr, "metabolism (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-WQ00QWRG-J
  skos:prefLabel "physiopathologie (Qualificatif)"@fr, "physiopathology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-DH7H9MJ2-N
  skos:prefLabel "anatomopathologie (Qualificatif)"@fr, "pathology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-MDQBX560-1
  skos:prefLabel "radiotherapy (Qualifier)"@en, "radiothérapie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-ZJBZVRWR-8
  skos:prefLabel "parasitologie (Qualificatif)"@fr, "parasitology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-W6T67RP3-2
  skos:prefLabel "diagnostic imaging (Qualifier)"@en, "imagerie diagnostique (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-B6C87218-T
  skos:prefLabel "prévention et contrôle (Qualificatif)"@fr, "prevention & control (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-QX850H97-1
  skos:prefLabel "Dyskeratosis Congenita"@en, "Dyskératose congénitale"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-ZWVQTNBQ-N
  skos:prefLabel "Hémophilie B"@fr, "Hemophilia B"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-BQ3W1P91-F
  skos:prefLabel "thérapie (Qualificatif)"@fr, "therapy (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-WCWMB697-P
  skos:prefLabel "Granulomatous Disease, Chronic"@en, "Granulomatose septique chronique"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-QPXST43W-0
  skos:prefLabel "Ornithine Carbamoyltransferase Deficiency Disease"@en, "Déficit en ornithine carbamyl transférase"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-KRXG97RR-5
  skos:prefLabel "diagnostic (Qualificatif)"@fr, "diagnosis (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-KQG0FKCK-3
  skos:prefLabel "Choroïdérémie"@fr, "Choroideremia"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-XP0SKMMB-8
  skos:prefLabel "Hyper-IgM Immunodeficiency Syndrome, Type 1"@en, "Syndrome d'hyper-IgM lié à l'X"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-HR1VJT6N-0
  skos:prefLabel "Amyotrophie bulbospinale liée à l'X"@fr, "Bulbo-Spinal Atrophy, X-Linked"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-X1V1J4G1-Q
  skos:prefLabel "Myopathie de Duchenne"@fr, "Muscular Dystrophy, Duchenne"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-J9Z93VFN-9
  skos:prefLabel "enzymology (Qualifier)"@en, "enzymologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-R490QF7F-9
  skos:prefLabel "Genetic Diseases, Inborn"@en, "Maladies génétiques congénitales"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-BL0Q8DS8-X .

jvr:-T1QJHLQ4-J
  skos:prefLabel "microbiology (Qualifier)"@en, "microbiologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-KFM33PF8-L
  skos:prefLabel "médecine vétérinaire (Qualificatif)"@fr, "veterinary (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr: a skos:ConceptScheme .
jvr:-BBD0S71C-R
  skos:prefLabel "induit chimiquement (Qualificatif)"@fr, "chemically induced (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-XVHTZRCG-7
  skos:prefLabel "étiologie (Qualificatif)"@fr, "etiology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-SDPG013V-D
  skos:prefLabel "psychology (Qualifier)"@en, "psychologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-T6JZ48ZV-N
  skos:prefLabel "complications (Qualifier)"@en, "complications (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-NXTG79SM-J
  skos:prefLabel "Isolated Noncompaction of the Ventricular Myocardium"@en, "Non-compaction isolée du ventricule"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-P1X8SCQ6-K
  skos:prefLabel "virologie (Qualificatif)"@fr, "virology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-V6VG3SXZ-9
  skos:prefLabel "Muscular Dystrophy, Emery-Dreifuss"@en, "Dystrophie musculaire d'Emery-Dreifuss"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-W6SQV79N-S
  skos:prefLabel "classification (Qualifier)"@en, "classification (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-G2D2FJXF-F
  skos:prefLabel "Dysplasie ectodermique anhidrotique de type 1"@fr, "Ectodermal Dysplasia 1, Anhidrotic"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-JJD15SB5-7
  skos:prefLabel "Maladie de Dent"@fr, "Dent Disease"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-GXVR9QN8-P
  skos:prefLabel "drug therapy (Qualifier)"@en, "traitement médicamenteux (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-L03WDG98-J
  skos:prefLabel "Fabry Disease"@en, "Maladie de Fabry"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-S0CS1X5R-5
  skos:prefLabel "immunology (Qualifier)"@en, "immunologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-CB30NGKB-3
  skos:prefLabel "economics (Qualifier)"@en, "économie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-M2R2GN6Z-S
  skos:prefLabel "Syndrome de Lowe"@fr, "Oculocerebrorenal Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-LN9D5D2P-Q
  skos:prefLabel "Sex Chromosome Aberrations"@en, "Aberrations des chromosomes sexuels"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-BL0Q8DS8-X .

jvr:-SC1LJ8FN-N
  skos:prefLabel "Immunodéficiences combinées graves liées à l'X"@fr, "X-Linked Combined Immunodeficiency Diseases"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-BT300B3G-Q
  skos:prefLabel "cerebrospinal fluid (Qualifier)"@en, "liquide cérébrospinal (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-CSKTXWF5-F
  skos:prefLabel "epidemiology (Qualifier)"@en, "épidémiologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-BL0Q8DS8-X
  mesh:allowableQualifier jvr:-T6JZ48ZV-N, jvr:-BT300B3G-Q, jvr:-S0CS1X5R-5, jvr:-RC3PND0F-S, jvr:-SBNWSM1T-R, jvr:-MDQBX560-1, jvr:-BBD0S71C-R, jvr:-SDPG013V-D, jvr:-BQ3W1P91-F, jvr:-KFM33PF8-L, jvr:-W4X1LN61-R, jvr:-HPKB70N8-W, jvr:-NHL3D2X0-S, jvr:-Z9TSGBXH-4, jvr:-P1X8SCQ6-K, jvr:-T1QJHLQ4-J, jvr:-CB30NGKB-3, jvr:-WQ00QWRG-J, jvr:-JVKFK2NX-2, jvr:-GXVR9QN8-P, jvr:-CSKTXWF5-F, jvr:-XV06LPML-W, jvr:-SDXQ5280-F, jvr:-B6C87218-T, jvr:-W6SQV79N-S, jvr:-W6T67RP3-2, jvr:-XVHTZRCG-7, jvr:-DH7H9MJ2-N, jvr:-J9Z93VFN-9, jvr:-L6C0XPHT-4, jvr:-VG20R78F-K, jvr:-WWJHCQRB-K, jvr:-KRXG97RR-5, jvr:-ZJBZVRWR-8 ;
  skos:narrower jvr:-QX850H97-1, jvr:-NNF6WD0C-X, jvr:-M2R2GN6Z-S, jvr:-VT4SSKPN-R, jvr:-KQG0FKCK-3, jvr:-V6VG3SXZ-9, jvr:-HR1VJT6N-0, jvr:-XP0SKMMB-8, jvr:-X1V1J4G1-Q, jvr:-ZWVQTNBQ-N, jvr:-DQKZFXBR-N, jvr:-JJD15SB5-7, jvr:-QPXST43W-0, jvr:-G2D2FJXF-F, jvr:-L03WDG98-J, jvr:-WCWMB697-P, jvr:-PKKTLP82-G, jvr:-D13J9255-9, jvr:-TPC7BCZB-K, jvr:-NXTG79SM-J, jvr:-QNTHSRJP-H, jvr:-SC1LJ8FN-N, jvr:-QGXF7H6W-Z, jvr:-MVS1D7T9-J ;
  skos:altLabel "Maladies liées à l'X"@fr, "Maladies portées par le chromosome X"@fr, "X-Linked Genetic Diseases"@en, "Genetic Diseases, X-Chromosome Linked"@en, "Maladies liées au chromosome X"@fr ;
  skos:related jvr:-QWPJH3S1-Q, jvr:-LN9D5D2P-Q, jvr:-MZSM0WD8-T, jvr:-R94PJZ29-W ;
  skos:definition "Genetic diseases that are linked to gene mutations on the X CHROMOSOME in humans (X CHROMOSOME, HUMAN) or the X CHROMOSOME in other species. Included here are animal models of human X-linked diseases."@en ;
  dc:created "2002-07-03"^^xsd:date ;
  a mesh:Descriptor, skos:Concept ;
  owl:sameAs <http://id.nlm.nih.gov/mesh/D040181> ;
  skos:prefLabel "Genetic Diseases, X-Linked"@en, "Maladies génétiques liées au chromosome X"@fr ;
  dc:modified "2013-07-09"^^xsd:date ;
  skos:broader jvr:-R490QF7F-9 ;
  dc:established "2003-01-01"^^xsd:date ;
  skos:inScheme jvr: .

jvr:-VT4SSKPN-R
  skos:prefLabel "Syndrome d'insensibilité aux androgènes"@fr, "Androgen-Insensitivity Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-JVKFK2NX-2
  skos:prefLabel "nursing (Qualifier)"@en, "soins infirmiers (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-D13J9255-9
  skos:prefLabel "Mental Retardation, X-Linked"@en, "Retard mental lié à l'X"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-W4X1LN61-R
  skos:prefLabel "diet therapy (Qualifier)"@en, "diétothérapie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-PKKTLP82-G
  skos:prefLabel "Barth Syndrome"@en, "Syndrome de Barth"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-DQKZFXBR-N
  skos:prefLabel "Maladie de Pelizaeus-Merzbacher"@fr, "Pelizaeus-Merzbacher Disease"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-QWPJH3S1-Q
  skos:prefLabel "Maladies liées aux chromosomes sexuels"@fr, "Sex Chromosome Disorders"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-BL0Q8DS8-X .

jvr:-QNTHSRJP-H
  skos:prefLabel "Ichthyosis, X-Linked"@en, "Ichtyose liée à l'X"@fr ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-RC3PND0F-S
  skos:prefLabel "ethnology (Qualifier)"@en, "ethnologie (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-TPC7BCZB-K
  skos:prefLabel "Hypoplasie dermique en aires"@fr, "Focal Dermal Hypoplasia"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-XV06LPML-W
  skos:prefLabel "urine (Qualifier)"@en, "urine (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .

jvr:-R94PJZ29-W
  skos:prefLabel "Chromosomes X humains"@fr, "Chromosomes, Human, X"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:related jvr:-BL0Q8DS8-X .

jvr:-NHL3D2X0-S
  skos:prefLabel "sang (Qualificatif)"@fr, "blood (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

jvr:-MVS1D7T9-J
  skos:prefLabel "Syndrome de Wiskott-Aldrich"@fr, "Wiskott-Aldrich Syndrome"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:broader jvr:-BL0Q8DS8-X .

jvr:-SBNWSM1T-R
  skos:prefLabel "history (Qualifier)"@en, "histoire (Qualificatif)"@fr ;
  a mesh:Qualifier, skos:Concept .