@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP44655.RAKksc4Cy527BxSwzDgK_oIwj7q7nAN45p5W26F3JF6wc> .
@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:NP44655.RAKksc4Cy527BxSwzDgK_oIwj7q7nAN45p5W26F3JF6wc130_head {
   this: np:hasAssertion dgn-np:NP44655.RAKksc4Cy527BxSwzDgK_oIwj7q7nAN45p5W26F3JF6wc130_assertion ;
    np:hasProvenance dgn-np:NP44655.RAKksc4Cy527BxSwzDgK_oIwj7q7nAN45p5W26F3JF6wc130_provenance ;
    np:hasPublicationInfo dgn-np:NP44655.RAKksc4Cy527BxSwzDgK_oIwj7q7nAN45p5W26F3JF6wc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP44655.RAKksc4Cy527BxSwzDgK_oIwj7q7nAN45p5W26F3JF6wc130_assertion a np:Assertion .
  dgn-np:NP44655.RAKksc4Cy527BxSwzDgK_oIwj7q7nAN45p5W26F3JF6wc130_provenance a np:Provenance .
  dgn-np:NP44655.RAKksc4Cy527BxSwzDgK_oIwj7q7nAN45p5W26F3JF6wc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP44655.RAKksc4Cy527BxSwzDgK_oIwj7q7nAN45p5W26F3JF6wc130_assertion {
   miriam-gene:2113 a ncit:C16612 .
  lld:C0024141 a ncit:C7057 .
  dgn-gda:DGNb94413e87b396f57a669b767e1793b00 sio:SIO_000628 miriam-gene:2113 , lld:C0024141 ;
    a sio:SIO_001122 .
}
dgn-np:NP44655.RAKksc4Cy527BxSwzDgK_oIwj7q7nAN45p5W26F3JF6wc130_provenance {
   dgn-np:NP44655.RAKksc4Cy527BxSwzDgK_oIwj7q7nAN45p5W26F3JF6wc130_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:NP44655.RAKksc4Cy527BxSwzDgK_oIwj7q7nAN45p5W26F3JF6wc130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:20+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" .
}