@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57867.RApCcgzLru2lxf2khwvs-sptk0ZLiFO8ezEwtVSkh9ocA> .
@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:NP57867.RApCcgzLru2lxf2khwvs-sptk0ZLiFO8ezEwtVSkh9ocA130_head {
  this: np:hasAssertion dgn-np:NP57867.RApCcgzLru2lxf2khwvs-sptk0ZLiFO8ezEwtVSkh9ocA130_assertion ;
    np:hasProvenance dgn-np:NP57867.RApCcgzLru2lxf2khwvs-sptk0ZLiFO8ezEwtVSkh9ocA130_provenance ;
    np:hasPublicationInfo dgn-np:NP57867.RApCcgzLru2lxf2khwvs-sptk0ZLiFO8ezEwtVSkh9ocA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP57867.RApCcgzLru2lxf2khwvs-sptk0ZLiFO8ezEwtVSkh9ocA130_assertion a np:Assertion .
  dgn-np:NP57867.RApCcgzLru2lxf2khwvs-sptk0ZLiFO8ezEwtVSkh9ocA130_provenance a np:Provenance .
  dgn-np:NP57867.RApCcgzLru2lxf2khwvs-sptk0ZLiFO8ezEwtVSkh9ocA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP57867.RApCcgzLru2lxf2khwvs-sptk0ZLiFO8ezEwtVSkh9ocA130_assertion {
  miriam-gene:3119 a ncit:C16612 .
  lld:C0024141 a ncit:C7057 .
  dgn-gda:DGN07811f93dd741cf2b78c73c7c5b83026 sio:SIO_000628 miriam-gene:3119 , lld:C0024141 ;
    a sio:SIO_001122 .
}
dgn-np:NP57867.RApCcgzLru2lxf2khwvs-sptk0ZLiFO8ezEwtVSkh9ocA130_provenance {
  dgn-np:NP57867.RApCcgzLru2lxf2khwvs-sptk0ZLiFO8ezEwtVSkh9ocA130_assertion dcterms:description "[The results suggest that the DRB1*0301 is the principal class II allele associated with the genetic susceptibility to SLE in Mexican patients and that the presence of a specific haplotype of the homologous chromosome in patients with DRB1*0407-DQA1*03-DQB1*0302 and DRB1*1501-DQA1*0102-DQB1*0602 haplotypes could have an additive effect on the susceptibility to the disease. Finally, the low frequency of the DRB1*0301 and DRB1*1501 alleles in the control population suggests that the genetic admixture between Mexican Indians and Caucasian populations was an event that could have increased the risk of Mexicans to develop SLE.]. 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:11476905 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP57867.RApCcgzLru2lxf2khwvs-sptk0ZLiFO8ezEwtVSkh9ocA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:27+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" .
}