@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_head {
  this: np:hasAssertion dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_assertion ;
    np:hasProvenance dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_provenance ;
    np:hasPublicationInfo dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_assertion a np:Assertion .
  dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_provenance a np:Provenance .
  dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_assertion {
  miriam-gene:4713 a ncit:C16612 .
  lld:C0011854 a ncit:C7057 .
  dgn-gda:DGN5a5a8f51a5562590837d217628c08b6a sio:SIO_000628 miriam-gene:4713 , lld:C0011854 ;
    a sio:SIO_001121 .
}
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_provenance {
  dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_assertion dcterms:description "[The extended HLA haplotype B18 CF130 DR3 DQw2, which is common (around 10% phenotype frequency) in healthy Spaniards and in other populations of paleo-North African origin, was found to be significantly less frequent in NIDD, JRA and BD, whereas its frequency was normal in IDD (although DR3 DQw2 haplotypes were increased in the latter disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
    sio:SIO_000772 miriam-pubmed:8335082 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  dgn-void:source_evidence_literature a eco:ECO_0000212 ;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:27+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
    dcterms:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269> , <http://orcid.org/0000-0002-7534-7661> , <http://orcid.org/0000-0002-9383-528X> , <http://orcid.org/0000-0003-0169-8159> , <http://orcid.org/0000-0003-1244-7654> ;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}