@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP413462.RAOQzeYulAvOeg9a4TZHDXpX5OWCZ5xIxoUVMZqORLybA> .
@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:NP413462.RAOQzeYulAvOeg9a4TZHDXpX5OWCZ5xIxoUVMZqORLybA130_head {
  this: np:hasAssertion dgn-np:NP413462.RAOQzeYulAvOeg9a4TZHDXpX5OWCZ5xIxoUVMZqORLybA130_assertion;
    np:hasProvenance dgn-np:NP413462.RAOQzeYulAvOeg9a4TZHDXpX5OWCZ5xIxoUVMZqORLybA130_provenance;
    np:hasPublicationInfo dgn-np:NP413462.RAOQzeYulAvOeg9a4TZHDXpX5OWCZ5xIxoUVMZqORLybA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP413462.RAOQzeYulAvOeg9a4TZHDXpX5OWCZ5xIxoUVMZqORLybA130_assertion a np:Assertion .
  
  dgn-np:NP413462.RAOQzeYulAvOeg9a4TZHDXpX5OWCZ5xIxoUVMZqORLybA130_provenance a np:Provenance .
  
  dgn-np:NP413462.RAOQzeYulAvOeg9a4TZHDXpX5OWCZ5xIxoUVMZqORLybA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP413462.RAOQzeYulAvOeg9a4TZHDXpX5OWCZ5xIxoUVMZqORLybA130_assertion {
  miriam-gene:4397 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN9170f66105185ecce8309ae52a61ea3a sio:SIO_000628 miriam-gene:4397, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP413462.RAOQzeYulAvOeg9a4TZHDXpX5OWCZ5xIxoUVMZqORLybA130_provenance {
  dgn-np:NP413462.RAOQzeYulAvOeg9a4TZHDXpX5OWCZ5xIxoUVMZqORLybA130_assertion dcterms:description
      "[These findings reveal a vital role for ICOS signaling in the generation and maintenance of human T(H)17 cells and suggest that components of this pathway could be therapeutically targeted to treat cancer or chronic infection and, conversely, that interruption of this pathway may have utility in multiple sclerosis and other autoimmune syndromes.]. 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:20980695;
    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:NP413462.RAOQzeYulAvOeg9a4TZHDXpX5OWCZ5xIxoUVMZqORLybA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:05+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" .
}