@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I> .
@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:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_head {
  this: np:hasAssertion dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_assertion;
    np:hasProvenance dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_provenance;
    np:hasPublicationInfo dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_assertion a np:Assertion .
  
  dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_provenance a np:Provenance .
  
  dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_assertion {
  miriam-gene:3558 a ncit:C16612 .
  
  lld:C0023895 a ncit:C7057 .
  
  dgn-gda:DGN651da2769d5e8624fe019b33f41d2617 sio:SIO_000628 miriam-gene:3558, lld:C0023895;
    a sio:SIO_001121 .
}

dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_provenance {
  dgn-np:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_assertion dcterms:description
      "[Considering the strong coincidence of primary sclerosing cholangitis (PSC) with UC and the increased frequency of other autoimmune disorders in patients with primary biliary cirrhosis (PBC), we investigated whether genetic variation in the IL2/IL21 region may also modulate the susceptibility to these two rare cholestatic liver diseases.]. 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:21304239;
    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:NP523350.RAAHgOH3fe9Ahx8KfcgeNFMm58vOVa-gqkoet3mX3093I130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:11+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" .
}