@prefix foaf:	<http://xmlns.com/foaf/0.1/> .
@prefix wikipedia-en:	<http://en.wikipedia.org/wiki/> .
@prefix dbr:	<http://dbpedia.org/resource/> .
wikipedia-en:RPGRIP1L	foaf:primaryTopic	dbr:RPGRIP1L .
@prefix dbo:	<http://dbpedia.org/ontology/> .
dbr:Microphthalmia	dbo:wikiPageWikiLink	dbr:RPGRIP1L .
dbr:C2_domain	dbo:wikiPageWikiLink	dbr:RPGRIP1L .
dbr:List_of_OMIM_disorder_codes	dbo:wikiPageWikiLink	dbr:RPGRIP1L .
dbr:List_of_genetic_disorders	dbo:wikiPageWikiLink	dbr:RPGRIP1L .
dbr:List_of_human_protein-coding_genes_3	dbo:wikiPageWikiLink	dbr:RPGRIP1L .
dbr:COACH_syndrome	dbo:wikiPageWikiLink	dbr:RPGRIP1L .
dbr:FTO_gene	dbo:wikiPageWikiLink	dbr:RPGRIP1L .
dbr:Joubert_syndrome	dbo:wikiPageWikiLink	dbr:RPGRIP1L .
dbr:Ciliopathy	dbo:wikiPageWikiLink	dbr:RPGRIP1L .
dbr:CUX1	dbo:wikiPageWikiLink	dbr:RPGRIP1L .
<http://dbpedia.org/resource/Meckel\u2013Gruber_syndrome>	dbo:wikiPageWikiLink	dbr:RPGRIP1L .
dbr:Syndromic_microphthalmia	dbo:wikiPageWikiLink	dbr:RPGRIP1L .
@prefix rdf:	<http://www.w3.org/1999/02/22-rdf-syntax-ns#> .
dbr:RPGRIP1L	rdf:type	dbo:Biomolecule ,
		dbo:Protein .
@prefix wikidata:	<http://www.wikidata.org/entity/> .
dbr:RPGRIP1L	rdf:type	wikidata:Q206229 ,
		wikidata:Q8054 .
@prefix owl:	<http://www.w3.org/2002/07/owl#> .
dbr:RPGRIP1L	rdf:type	owl:Thing ;
	owl:sameAs	wikidata:Q24722012 ,
		<https://global.dbpedia.org/id/2KjiR> ,
		dbr:RPGRIP1L ,
		<http://rdf.freebase.com/ns/m.04n009j> .
@prefix dbpedia-ar:	<http://ar.dbpedia.org/resource/> .
dbr:RPGRIP1L	owl:sameAs	dbpedia-ar:RPGRIP1L ;
	foaf:name	"RPGRIP1-like"@en .
@prefix rdfs:	<http://www.w3.org/2000/01/rdf-schema#> .
dbr:RPGRIP1L	rdfs:label	"RPGRIP1L"@ar ,
		"RPGRIP1L"@en .
@prefix prov:	<http://www.w3.org/ns/prov#> .
dbr:RPGRIP1L	prov:wasDerivedFrom	<http://en.wikipedia.org/wiki/RPGRIP1L?oldid=1223134790&ns=0> ;
	dbo:wikiPageWikiLink	dbr:FTO_gene ,
		dbr:NPHP4 ,
		dbr:Leptin ,
		dbr:Centrosome ,
		dbr:Hypothalamus ,
		dbr:Autosomal_recessive ,
		dbr:Microtubule_nucleation ,
		dbr:Nephronophthisis ,
		dbr:Copy_number_variation ,
		dbr:Meckel_syndrome ,
		dbr:Cilia ,
		dbr:Cilium ,
		dbr:Schizophrenia ,
		dbr:Joubert_syndrome ,
		dbr:NPHP6 ,
		dbr:Gene ;
	dbo:description	"famille InterPro"@fr ,
		"Proteinfamilie"@de ,
		"InterPro Family"@en ,
		"InterPro \u0568\u0576\u057F\u0561\u0576\u056B\u0584"@hy ,
		"eiwitfamilie"@nl ,
		"\u0440\u043E\u0434\u0438\u043D\u0430 \u0431\u0456\u043B\u043A\u0456\u0432"@uk .
@prefix dbp:	<http://dbpedia.org/property/> .
@prefix dbt:	<http://dbpedia.org/resource/Template:> .
dbr:RPGRIP1L	dbp:wikiPageUsesTemplate	dbt:Gene-16-stub ,
		dbt:Infobox_protein ,
		dbt:Ciliary_proteins ,
		dbt:Reflist ,
		dbt:Short_description ;
	dbp:name	"RPGRIP1-like"@en ;
	dbp:omim	610937 ;
	dbo:omim	610937 ;
	dbo:uniprot	"Q68CZ1" ;
	dbo:arm	"q" ;
	dbo:band	"12.2" ;
	dbo:chromosome	"16" ;
	dbo:entrezgene	"23322" ;
	dbo:hgncid	"29168" ;
	dbo:refseq	"NM_015272" .
@prefix gold:	<http://purl.org/linguistics/gold/> .
dbr:RPGRIP1L	gold:hypernym	dbr:Gene ;
	foaf:isPrimaryTopicOf	wikipedia-en:RPGRIP1L .
@prefix xsd:	<http://www.w3.org/2001/XMLSchema#> .
dbr:RPGRIP1L	dbp:band	"12.2"^^xsd:double ;
	dbo:symbol	"NPHP8, KIAA1005, CORS3, JBTS7, MKS5, FTM" ,
		"RPGRIP1L" ;
	dbp:hgncid	29168 ;
	dbp:arm	"q"@en ;
	dbp:uniprot	"Q68CZ1"@en ;
	dbp:altsymbols	"NPHP8, KIAA1005, CORS3, JBTS7, MKS5, FTM"@en ;
	dbp:refseq	"NM_015272"@en ;
	dbp:entrezgene	23322 ;
	dbp:chromosome	16 ;
	dbp:symbol	"RPGRIP1L"@en .
dbr:NPHP8	dbo:wikiPageWikiLink	dbr:RPGRIP1L ;
	dbo:wikiPageRedirects	dbr:RPGRIP1L .