@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP622999.RA9tkUJnaduO-cChmGS6AqzIE-VM5jtLTXc072lXNWngU> .
@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:NP622999.RA9tkUJnaduO-cChmGS6AqzIE-VM5jtLTXc072lXNWngU130_head {
  this: np:hasAssertion dgn-np:NP622999.RA9tkUJnaduO-cChmGS6AqzIE-VM5jtLTXc072lXNWngU130_assertion;
    np:hasProvenance dgn-np:NP622999.RA9tkUJnaduO-cChmGS6AqzIE-VM5jtLTXc072lXNWngU130_provenance;
    np:hasPublicationInfo dgn-np:NP622999.RA9tkUJnaduO-cChmGS6AqzIE-VM5jtLTXc072lXNWngU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP622999.RA9tkUJnaduO-cChmGS6AqzIE-VM5jtLTXc072lXNWngU130_assertion a np:Assertion .
  
  dgn-np:NP622999.RA9tkUJnaduO-cChmGS6AqzIE-VM5jtLTXc072lXNWngU130_provenance a np:Provenance .
  
  dgn-np:NP622999.RA9tkUJnaduO-cChmGS6AqzIE-VM5jtLTXc072lXNWngU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP622999.RA9tkUJnaduO-cChmGS6AqzIE-VM5jtLTXc072lXNWngU130_assertion {
  miriam-gene:3439 a ncit:C16612 .
  
  lld:C0010823 a ncit:C7057 .
  
  dgn-gda:DGN1bdc50f9f23e28a29249ef39f9f065ba sio:SIO_000628 miriam-gene:3439, lld:C0010823;
    a sio:SIO_001121 .
}

dgn-np:NP622999.RA9tkUJnaduO-cChmGS6AqzIE-VM5jtLTXc072lXNWngU130_provenance {
  dgn-np:NP622999.RA9tkUJnaduO-cChmGS6AqzIE-VM5jtLTXc072lXNWngU130_assertion dcterms:description
      "[The specific subtype gene of type I IFN, the DNA concentration, the combined use of two or more subtypes, and the timing of the DNA immunisations were all found to influence the level of efficacy of IFN gene therapy in a mouse model for cytomegalovirus (CMV) infection and disease.]. 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:16000864;
    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:NP622999.RA9tkUJnaduO-cChmGS6AqzIE-VM5jtLTXc072lXNWngU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:16+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" .
}