@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o> .
@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:NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130_head {
  this: np:hasAssertion dgn-np:NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130_assertion;
    np:hasProvenance dgn-np:NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130_provenance;
    np:hasPublicationInfo dgn-np:NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130_assertion a np:Assertion .
  
  dgn-np:NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130_provenance a np:Provenance .
  
  dgn-np:NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130_assertion {
  miriam-gene:2532 a ncit:C16612 .
  
  lld:C0004943 a ncit:C7057 .
  
  dgn-gda:DGN00ca3f987ca80a1511002c00f413738c sio:SIO_000628 miriam-gene:2532, lld:C0004943;
    a sio:SIO_001122 .
}

dgn-np:NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130_provenance {
  dgn-np:NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130_assertion dcterms:description
      "[This investigation indicates that DARC is not a genetic trait significantly associated with or predisposing to Behcet's disease, at least in Caucasian Italians. However, the role of this polymorphism in the development and in the clinical course of the disease awaits further investigation.]. 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:12739041;
    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:NP67197.RAReaaQV8SbfXKaWv6N-1pZiWfPt51NffSpvmt-mxWR1o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:32+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" .
}