@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP334565.RAy5yEi7QFkCnALYxVXTIWYbbbiL2BtejKGr7XbJYOnk0> .
@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:NP334565.RAy5yEi7QFkCnALYxVXTIWYbbbiL2BtejKGr7XbJYOnk0130_head {
  this: np:hasAssertion dgn-np:NP334565.RAy5yEi7QFkCnALYxVXTIWYbbbiL2BtejKGr7XbJYOnk0130_assertion;
    np:hasProvenance dgn-np:NP334565.RAy5yEi7QFkCnALYxVXTIWYbbbiL2BtejKGr7XbJYOnk0130_provenance;
    np:hasPublicationInfo dgn-np:NP334565.RAy5yEi7QFkCnALYxVXTIWYbbbiL2BtejKGr7XbJYOnk0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP334565.RAy5yEi7QFkCnALYxVXTIWYbbbiL2BtejKGr7XbJYOnk0130_assertion a np:Assertion .
  
  dgn-np:NP334565.RAy5yEi7QFkCnALYxVXTIWYbbbiL2BtejKGr7XbJYOnk0130_provenance a np:Provenance .
  
  dgn-np:NP334565.RAy5yEi7QFkCnALYxVXTIWYbbbiL2BtejKGr7XbJYOnk0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP334565.RAy5yEi7QFkCnALYxVXTIWYbbbiL2BtejKGr7XbJYOnk0130_assertion {
  miriam-gene:6622 a ncit:C16612 .
  
  lld:C0024141 a ncit:C7057 .
  
  dgn-gda:DGN6059d52b71e1505637daf9c112f1d93b sio:SIO_000628 miriam-gene:6622, lld:C0024141;
    a sio:SIO_001121 .
}

dgn-np:NP334565.RAy5yEi7QFkCnALYxVXTIWYbbbiL2BtejKGr7XbJYOnk0130_provenance {
  dgn-np:NP334565.RAy5yEi7QFkCnALYxVXTIWYbbbiL2BtejKGr7XbJYOnk0130_assertion dcterms:description
      "[These results cast doubts on the functional relevance of the PD1.3 SNP and, together with the lack of association in several studies, put into question its role as an SLE susceptibility factor.]. 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:18401354;
    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:NP334565.RAy5yEi7QFkCnALYxVXTIWYbbbiL2BtejKGr7XbJYOnk0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:17+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>;
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    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}