@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP841153.RA-g58T70b6Ro9oTmKnaS7gnhrVwCL7Tggryn4f2v2psA> .
@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:NP841153.RA-g58T70b6Ro9oTmKnaS7gnhrVwCL7Tggryn4f2v2psA130_head {
   this: np:hasAssertion dgn-np:NP841153.RA-g58T70b6Ro9oTmKnaS7gnhrVwCL7Tggryn4f2v2psA130_assertion ;
    np:hasProvenance dgn-np:NP841153.RA-g58T70b6Ro9oTmKnaS7gnhrVwCL7Tggryn4f2v2psA130_provenance ;
    np:hasPublicationInfo dgn-np:NP841153.RA-g58T70b6Ro9oTmKnaS7gnhrVwCL7Tggryn4f2v2psA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP841153.RA-g58T70b6Ro9oTmKnaS7gnhrVwCL7Tggryn4f2v2psA130_assertion a np:Assertion .
  dgn-np:NP841153.RA-g58T70b6Ro9oTmKnaS7gnhrVwCL7Tggryn4f2v2psA130_provenance a np:Provenance .
  dgn-np:NP841153.RA-g58T70b6Ro9oTmKnaS7gnhrVwCL7Tggryn4f2v2psA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP841153.RA-g58T70b6Ro9oTmKnaS7gnhrVwCL7Tggryn4f2v2psA130_assertion {
   miriam-gene:2113 a ncit:C16612 .
  lld:C0014060 a ncit:C7057 .
  dgn-gda:DGN4de1fffb3e3c63b5d3ea6e08297e7629 sio:SIO_000628 miriam-gene:2113 , lld:C0014060 ;
    a sio:SIO_001121 .
}
dgn-np:NP841153.RA-g58T70b6Ro9oTmKnaS7gnhrVwCL7Tggryn4f2v2psA130_provenance {
   dgn-np:NP841153.RA-g58T70b6Ro9oTmKnaS7gnhrVwCL7Tggryn4f2v2psA130_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: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:NP841153.RA-g58T70b6Ro9oTmKnaS7gnhrVwCL7Tggryn4f2v2psA130_publicationInfo {
   this: dcterms:created "2014-10-02T12:40:34+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" .
}