@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP182420.RA7eWf5E_Pb5riLR_jVRMbfQMus9Ehk4utFArHCKoAKjE> .
@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:NP182420.RA7eWf5E_Pb5riLR_jVRMbfQMus9Ehk4utFArHCKoAKjE130_head {
  this: np:hasAssertion dgn-np:NP182420.RA7eWf5E_Pb5riLR_jVRMbfQMus9Ehk4utFArHCKoAKjE130_assertion;
    np:hasProvenance dgn-np:NP182420.RA7eWf5E_Pb5riLR_jVRMbfQMus9Ehk4utFArHCKoAKjE130_provenance;
    np:hasPublicationInfo dgn-np:NP182420.RA7eWf5E_Pb5riLR_jVRMbfQMus9Ehk4utFArHCKoAKjE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP182420.RA7eWf5E_Pb5riLR_jVRMbfQMus9Ehk4utFArHCKoAKjE130_assertion a np:Assertion .
  
  dgn-np:NP182420.RA7eWf5E_Pb5riLR_jVRMbfQMus9Ehk4utFArHCKoAKjE130_provenance a np:Provenance .
  
  dgn-np:NP182420.RA7eWf5E_Pb5riLR_jVRMbfQMus9Ehk4utFArHCKoAKjE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP182420.RA7eWf5E_Pb5riLR_jVRMbfQMus9Ehk4utFArHCKoAKjE130_assertion {
  miriam-gene:2952 a ncit:C16612 .
  
  lld:C0023467 a ncit:C7057 .
  
  dgn-gda:DGN88a3ebfd97151f1c9588c2e8ab986810 sio:SIO_000628 miriam-gene:2952, lld:C0023467;
    a sio:SIO_001121 .
}

dgn-np:NP182420.RA7eWf5E_Pb5riLR_jVRMbfQMus9Ehk4utFArHCKoAKjE130_provenance {
  dgn-np:NP182420.RA7eWf5E_Pb5riLR_jVRMbfQMus9Ehk4utFArHCKoAKjE130_assertion dcterms:description
      "[We used the allelic discrimination method to identify polymorphisms in GSTT1, SULT1C2, CDA, SXR (drug metabolic pathways), XPD, XPA, XPG, ERCC1, TOP2A (DNA repair), VEGF (angiogenesis), and MDR1 (multidrug resistance) genes in 110 adult patients with intermediate-risk AML, enrolled in the CETLAM-99 prospective trial.]. 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:16507781;
    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:NP182420.RA7eWf5E_Pb5riLR_jVRMbfQMus9Ehk4utFArHCKoAKjE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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" .
}