@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP82745.RAAi7DvUC_rYTI7A0PzkdAqGrZnE9KKEmn9OAhMQyCV0c> .
@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:NP82745.RAAi7DvUC_rYTI7A0PzkdAqGrZnE9KKEmn9OAhMQyCV0c130_head {
   this: np:hasAssertion dgn-np:NP82745.RAAi7DvUC_rYTI7A0PzkdAqGrZnE9KKEmn9OAhMQyCV0c130_assertion ;
    np:hasProvenance dgn-np:NP82745.RAAi7DvUC_rYTI7A0PzkdAqGrZnE9KKEmn9OAhMQyCV0c130_provenance ;
    np:hasPublicationInfo dgn-np:NP82745.RAAi7DvUC_rYTI7A0PzkdAqGrZnE9KKEmn9OAhMQyCV0c130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP82745.RAAi7DvUC_rYTI7A0PzkdAqGrZnE9KKEmn9OAhMQyCV0c130_assertion a np:Assertion .
  dgn-np:NP82745.RAAi7DvUC_rYTI7A0PzkdAqGrZnE9KKEmn9OAhMQyCV0c130_provenance a np:Provenance .
  dgn-np:NP82745.RAAi7DvUC_rYTI7A0PzkdAqGrZnE9KKEmn9OAhMQyCV0c130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP82745.RAAi7DvUC_rYTI7A0PzkdAqGrZnE9KKEmn9OAhMQyCV0c130_assertion {
   miriam-gene:57705 a ncit:C16612 .
  lld:C0024141 a ncit:C7057 .
  dgn-gda:DGN80cc5ce47e92d4a1080978091bbc44ca sio:SIO_000628 miriam-gene:57705 , lld:C0024141 ;
    a sio:SIO_001122 .
}
dgn-np:NP82745.RAAi7DvUC_rYTI7A0PzkdAqGrZnE9KKEmn9OAhMQyCV0c130_provenance {
   dgn-np:NP82745.RAAi7DvUC_rYTI7A0PzkdAqGrZnE9KKEmn9OAhMQyCV0c130_assertion dcterms:description "[By a genome-wide association study (320 patients and 1,500 controls) and subsequent replication altogether involving a total of 3,300 Asian SLE patients from Hong Kong, Mainland China, and Thailand, as well as 4,200 ethnically and geographically matched controls, genetic variants in ETS1 and WDFY4 were found to be associated with SLE (ETS1: rs1128334, P = 2.33x10(-11), OR = 1.29; WDFY4: rs7097397, P = 8.15x10(-12), OR = 1.30).]. 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:20169177 ;
    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:NP82745.RAAi7DvUC_rYTI7A0PzkdAqGrZnE9KKEmn9OAhMQyCV0c130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:40+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" .
}