@prefix foaf:	<http://xmlns.com/foaf/0.1/> .
@prefix wikipedia-en:	<http://en.wikipedia.org/wiki/> .
@prefix ns2:	<https://dbpedia.org/resource/> .
wikipedia-en:H_syndrome	foaf:primaryTopic	ns2:H_syndrome .
@prefix ns3:	<https://dbpedia.org/ontology/> .
ns2:Dysosteosclerosis	ns3:wikiPageWikiLink	ns2:H_syndrome .
@prefix rdf:	<http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
@prefix wikidata:	<http://www.wikidata.org/entity/> .
ns2:H_syndrome	rdf:type	wikidata:Q12136 .
@prefix owl:	<http://www.w3.org/2002/07/owl#> .
ns2:H_syndrome	rdf:type	owl:Thing ,
		ns3:Disease ;
	owl:sameAs	<https://global.dbpedia.org/id/2wDNJ> .
@prefix dbpedia-de:	<http://de.dbpedia.org/resource/> .
ns2:H_syndrome	owl:sameAs	dbpedia-de:H-Syndrom ,
		wikidata:Q31841284 .
@prefix dbr:	<http://dbpedia.org/resource/> .
ns2:H_syndrome	owl:sameAs	dbr:H_syndrome ;
	foaf:name	"H syndrome"@en .
@prefix rdfs:	<http://www.w3.org/2000/01/rdf-schema#> .
ns2:H_syndrome	rdfs:label	"H syndrome"@en ,
		"H-Syndrom"@de .
@prefix dct:	<http://purl.org/dc/terms/> .
@prefix ns11:	<https://dbpedia.org/resource/Category:> .
ns2:H_syndrome	dct:subject	ns11:Genetic_syndromes ,
		ns11:Rare_syndromes ,
		ns11:Autosomal_recessive_disorders ;
	foaf:depiction	<http://commons.wikimedia.org/wiki/Special:FilePath/Autosomal_recessive_-_en.svg> .
@prefix prov:	<http://www.w3.org/ns/prov#> .
ns2:H_syndrome	prov:wasDerivedFrom	<http://en.wikipedia.org/wiki/H_syndrome?oldid=1250790395&ns=0> ;
	foaf:isPrimaryTopicOf	wikipedia-en:H_syndrome ;
	ns3:wikiPageWikiLink	ns2:Hyperpigmentation ,
		ns2:Diabetes_mellitus ,
		ns11:Rare_syndromes ,
		ns2:Hepatosplenomegaly ,
		ns2:Exophthalmos ,
		ns2:Hypogonadism ,
		ns11:Autosomal_recessive_disorders ,
		ns11:Genetic_diseases_and_disorders ,
		ns2:Hallux_valgus ,
		ns2:SLC29A3 ,
		ns2:Hyperglycemia ,
		ns2:Hypertrichosis ,
		ns2:Malabsorption ;
	ns3:description	"genetic condition"@en .
@prefix ns13:	<https://dbpedia.org/property/> .
@prefix ns14:	<https://dbpedia.org/resource/Template:> .
ns2:H_syndrome	ns13:wikiPageUsesTemplate	ns14:Primary_sources ,
		ns14:Reflist ,
		ns14:Medical_resources ,
		ns14:Empty_section ,
		<https://dbpedia.org/resource/Template:Infobox_medical_condition_(new)> ,
		ns14:Cn ;
	ns13:name	"H syndrome"@en ;
	ns3:omim	602782 ;
	ns13:omim	602782 ;
	ns13:synonyms	"Histiocytosis-lymphadenopathy plus syndrome"@en ;
	ns13:caption	"This condition is inherited in an autosomal recessive manner"@en ;
	ns3:thumbnail	<http://commons.wikimedia.org/wiki/Special:FilePath/Autosomal_recessive_-_en.svg?width=300> .
ns2:Equilibrative_nucleoside_transporter_1	ns3:wikiPageWikiLink	ns2:H_syndrome .