@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8_fy_ClNjzqS81h8> .
@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:NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8_fy_ClNjzqS81h8130_head {
  this: np:hasAssertion dgn-np:NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8_fy_ClNjzqS81h8130_assertion;
    np:hasProvenance dgn-np:NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8_fy_ClNjzqS81h8130_provenance;
    np:hasPublicationInfo dgn-np:NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8_fy_ClNjzqS81h8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8_fy_ClNjzqS81h8130_assertion a np:Assertion .
  
  dgn-np:NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8_fy_ClNjzqS81h8130_provenance a np:Provenance .
  
  dgn-np:NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8_fy_ClNjzqS81h8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8_fy_ClNjzqS81h8130_assertion {
  miriam-gene:3458 a ncit:C16612 .
  
  lld:C0003873 a ncit:C7057 .
  
  dgn-gda:DGNc00ef8f2a1d9ab126570cd45c8624123 sio:SIO_000628 miriam-gene:3458, lld:C0003873;
    a sio:SIO_001122 .
}

dgn-np:NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8_fy_ClNjzqS81h8130_provenance {
  dgn-np:NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8_fy_ClNjzqS81h8130_assertion dcterms:description
      "[ Our results demonstrate that common polymorphisms in the IFNgamma/IL-26 gene region may contribute to sex bias in susceptibility to RA, by distorting the propensity of female carriers versus male carriers to contract this disease. These results conform to our recent observations of a role for this gene cluster in sex-based differential susceptibility to another Th1-type inflammatory disease, multiple sclerosis.]. 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:14558082;
    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:NP57014.RARvb-2VqBVKR3wl2GmBb1xHkQIZL8_fy_ClNjzqS81h8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:26+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" .
}