@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP59449.RAcgd40GLEL1MQI-StQ_PCMn29QZAjTWE_5Em4qNTprQs> .
@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:NP59449.RAcgd40GLEL1MQI-StQ_PCMn29QZAjTWE_5Em4qNTprQs130_head {
  this: np:hasAssertion dgn-np:NP59449.RAcgd40GLEL1MQI-StQ_PCMn29QZAjTWE_5Em4qNTprQs130_assertion;
    np:hasProvenance dgn-np:NP59449.RAcgd40GLEL1MQI-StQ_PCMn29QZAjTWE_5Em4qNTprQs130_provenance;
    np:hasPublicationInfo dgn-np:NP59449.RAcgd40GLEL1MQI-StQ_PCMn29QZAjTWE_5Em4qNTprQs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP59449.RAcgd40GLEL1MQI-StQ_PCMn29QZAjTWE_5Em4qNTprQs130_assertion a np:Assertion .
  
  dgn-np:NP59449.RAcgd40GLEL1MQI-StQ_PCMn29QZAjTWE_5Em4qNTprQs130_provenance a np:Provenance .
  
  dgn-np:NP59449.RAcgd40GLEL1MQI-StQ_PCMn29QZAjTWE_5Em4qNTprQs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP59449.RAcgd40GLEL1MQI-StQ_PCMn29QZAjTWE_5Em4qNTprQs130_assertion {
  miriam-gene:7515 a ncit:C16612 .
  
  lld:C0025202 a ncit:C7057 .
  
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    a sio:SIO_001122 .
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dgn-np:NP59449.RAcgd40GLEL1MQI-StQ_PCMn29QZAjTWE_5Em4qNTprQs130_provenance {
  dgn-np:NP59449.RAcgd40GLEL1MQI-StQ_PCMn29QZAjTWE_5Em4qNTprQs130_assertion dcterms:description
      "[ Cytokine gene polymorphisms predicted clinical outcome for advanced melanoma patients who received biochemotherapy. The combined effects of multiple genetic polymorphisms may provide more accurate prognostic information. Additional independent studies are needed to confirm these pilot findings.]. 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:15709194;
    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:NP59449.RAcgd40GLEL1MQI-StQ_PCMn29QZAjTWE_5Em4qNTprQs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:28+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" .
}