@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 owl: <http://www.w3.org/2002/07/owl#> .
@prefix dc: <http://purl.org/dc/terms/> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .

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

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

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

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

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:-VJ1M4GRP-0 .

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

jvr:-P31C9JZH-X
  skos:prefLabel "congénital (Qualificatif)"@fr, "congenital (Qualifier)"@en ;
  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:-P1X8SCQ6-K
  skos:prefLabel "virologie (Qualificatif)"@fr, "virology (Qualifier)"@en ;
  a mesh:Qualifier, skos:Concept .

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

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

jvr:-SXJP797G-D
  skos:prefLabel "Hyperthyroxinémie"@fr, "Hyperthyroxinemia"@en ;
  a mesh:Descriptor, skos:Concept ;
  skos:narrower jvr:-VJ1M4GRP-0 .

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

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

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

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

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

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

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

jvr:-VJ1M4GRP-0
  mesh:allowableQualifier jvr:-SBNWSM1T-R, jvr:-DH7H9MJ2-N, jvr:-B6C87218-T, jvr:-XVHTZRCG-7, jvr:-KRXG97RR-5, jvr:-L6C0XPHT-4, jvr:-MDQBX560-1, jvr:-W6T67RP3-2, jvr:-SDXQ5280-F, jvr:-S0CS1X5R-5, jvr:-KFM33PF8-L, jvr:-P31C9JZH-X, jvr:-Z9TSGBXH-4, jvr:-RC3PND0F-S, jvr:-SDPG013V-D, jvr:-XV06LPML-W, jvr:-WWJHCQRB-K, jvr:-CSKTXWF5-F, jvr:-CB30NGKB-3, jvr:-T1QJHLQ4-J, jvr:-WQ00QWRG-J, jvr:-T6JZ48ZV-N, jvr:-VG20R78F-K, jvr:-W4X1LN61-R, jvr:-BQ3W1P91-F, jvr:-W6SQV79N-S, jvr:-JVKFK2NX-2, jvr:-GXVR9QN8-P, jvr:-HPKB70N8-W, jvr:-NHL3D2X0-S, jvr:-BBD0S71C-R, jvr:-P1X8SCQ6-K, jvr:-BT300B3G-Q, jvr:-ZJBZVRWR-8, jvr:-J9Z93VFN-9 ;
  skos:prefLabel "Hyperthyroxinemia, Familial Dysalbuminemic"@en, "Hyperthyroxinémie dysalbuminémique familiale"@fr ;
  skos:definition "An inherited autosomal dominant trait characterized by abnormally elevated levels of total serum THYROXINE; (T4) in euthyroid patients with abnormal SERUM ALBUMIN that binds T4 with enhanced affinity. The serum levels of free T4, free T3, and TSH are normal. It is one of several T4 abnormalities produced by non-thyroid disorder. This condition is due to mutations of the ALB gene on CHROMOSOME 4."@en ;
  owl:sameAs <http://id.nlm.nih.gov/mesh/D050010> ;
  dc:modified "2005-08-02"^^xsd:date ;
  skos:broader jvr:-SXJP797G-D, jvr:-R490QF7F-9 ;
  dc:created "2005-06-30"^^xsd:date ;
  skos:altLabel "Familial Dysalbuminemic Hyperthyroxinemia"@en ;
  a skos:Concept, mesh:Descriptor ;
  dc:established "2006-01-01"^^xsd:date ;
  skos:inScheme jvr: .

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

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

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