@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To> .
@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:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_head {
  this: np:hasAssertion dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_assertion;
    np:hasProvenance dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_provenance;
    np:hasPublicationInfo dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_assertion a np:Assertion .
  
  dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_provenance a np:Provenance .
  
  dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGN088c35d4c50dbb91cc9879c243ba437d sio:SIO_000628 miriam-gene:2944, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_provenance {
  dgn-np:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_assertion dcterms:description
      "[The work studied possible association between genetic polymorphisms of CYP2D6, GSTM1, GSTT1and NQO1 and altered susceptibility to leukaemia, correlating these genetic polymorphisms with clinical prognostic data, response to therapy and relapse.]. 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:17581325;
    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:NP295674.RAThcMvnv6O2YPjf6ig5GCuYZQJkBElqms8UGZvjb12To130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:48+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" .
}