@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP71970.RA0NoyptrkPcfXUeljlW3djhuBPZ7KhwFZpUFQbNuKdKc> .
@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:NP71970.RA0NoyptrkPcfXUeljlW3djhuBPZ7KhwFZpUFQbNuKdKc130_head {
  this: np:hasAssertion dgn-np:NP71970.RA0NoyptrkPcfXUeljlW3djhuBPZ7KhwFZpUFQbNuKdKc130_assertion;
    np:hasProvenance dgn-np:NP71970.RA0NoyptrkPcfXUeljlW3djhuBPZ7KhwFZpUFQbNuKdKc130_provenance;
    np:hasPublicationInfo dgn-np:NP71970.RA0NoyptrkPcfXUeljlW3djhuBPZ7KhwFZpUFQbNuKdKc130_publicationInfo;
    a np:Nanopublication .
  
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  dgn-np:NP71970.RA0NoyptrkPcfXUeljlW3djhuBPZ7KhwFZpUFQbNuKdKc130_provenance a np:Provenance .
  
  dgn-np:NP71970.RA0NoyptrkPcfXUeljlW3djhuBPZ7KhwFZpUFQbNuKdKc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP71970.RA0NoyptrkPcfXUeljlW3djhuBPZ7KhwFZpUFQbNuKdKc130_assertion {
  miriam-gene:3569 a ncit:C16612 .
  
  lld:C0031106 a ncit:C7057 .
  
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dgn-np:NP71970.RA0NoyptrkPcfXUeljlW3djhuBPZ7KhwFZpUFQbNuKdKc130_provenance {
  dgn-np:NP71970.RA0NoyptrkPcfXUeljlW3djhuBPZ7KhwFZpUFQbNuKdKc130_assertion dcterms:description
      "[The aims of this study were to estimate the percentage of affected relatives of AgP individuals, to analyse the disease phenotypes in relatives and to explore the distributions of genetic polymorphisms of interleukin-6 (IL-6) in AgP patients and in diseased and healthy relatives.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP71970.RA0NoyptrkPcfXUeljlW3djhuBPZ7KhwFZpUFQbNuKdKc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:35+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
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  dgn-void:disgenetrdf pav:version "v2.1.0" .
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