@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk> .
@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:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_head {
  this: np:hasAssertion dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_assertion;
    np:hasProvenance dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_provenance;
    np:hasPublicationInfo dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_assertion a np:Assertion .
  
  dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_provenance a np:Provenance .
  
  dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_assertion {
  miriam-gene:2209 a ncit:C16612 .
  
  lld:C0151449 a ncit:C7057 .
  
  dgn-gda:DGN09b74f4e2e1a3a19e052a350eff761d5 sio:SIO_000628 miriam-gene:2209, lld:C0151449;
    a sio:SIO_001121 .
}

dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_provenance {
  dgn-np:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_assertion dcterms:description
      "[The lack of association of pSS with Fcγ receptor gene variants indicates that defective immune complex clearance may not be as important in pSS pathogenesis as in SLE, and may point to important differences between SLE and pSS.]. 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:23552400;
    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:NP341952.RAzXncEn9icoY71OI7j2BO3Ew-_u6oS4XIUgpu3mUOyMk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:21+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" .
}