@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP187974.RACc_uZWXaSCftglBSUiiWq65Hc0UyHgzTDnZZSaXN-mM> .
@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:NP187974.RACc_uZWXaSCftglBSUiiWq65Hc0UyHgzTDnZZSaXN-mM130_head {
  this: np:hasAssertion dgn-np:NP187974.RACc_uZWXaSCftglBSUiiWq65Hc0UyHgzTDnZZSaXN-mM130_assertion;
    np:hasProvenance dgn-np:NP187974.RACc_uZWXaSCftglBSUiiWq65Hc0UyHgzTDnZZSaXN-mM130_provenance;
    np:hasPublicationInfo dgn-np:NP187974.RACc_uZWXaSCftglBSUiiWq65Hc0UyHgzTDnZZSaXN-mM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP187974.RACc_uZWXaSCftglBSUiiWq65Hc0UyHgzTDnZZSaXN-mM130_assertion a np:Assertion .
  
  dgn-np:NP187974.RACc_uZWXaSCftglBSUiiWq65Hc0UyHgzTDnZZSaXN-mM130_provenance a np:Provenance .
  
  dgn-np:NP187974.RACc_uZWXaSCftglBSUiiWq65Hc0UyHgzTDnZZSaXN-mM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP187974.RACc_uZWXaSCftglBSUiiWq65Hc0UyHgzTDnZZSaXN-mM130_assertion {
  miriam-gene:7133 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGNf706187b3e22dfa429cc09ea988fd1ff sio:SIO_000628 miriam-gene:7133, lld:C0024141;
    a sio:SIO_001121 .
}

dgn-np:NP187974.RACc_uZWXaSCftglBSUiiWq65Hc0UyHgzTDnZZSaXN-mM130_provenance {
  dgn-np:NP187974.RACc_uZWXaSCftglBSUiiWq65Hc0UyHgzTDnZZSaXN-mM130_assertion dcterms:description
      "[Several new associations have been disclosed, including those of TNFR2, FCGR2B, and CD19 gene polymorphisms with systemic lupus erythematosus, in addition to some unexpected findings such as the common occurrence of NKG2-C null allele in the healthy population.]. 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:12493014;
    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:NP187974.RACc_uZWXaSCftglBSUiiWq65Hc0UyHgzTDnZZSaXN-mM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:43+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" .
}