@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE> .
@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:NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_head {
   this: np:hasAssertion dgn-np:NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_assertion ;
    np:hasProvenance dgn-np:NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance ;
    np:hasPublicationInfo dgn-np:NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_assertion a np:Assertion .
  dgn-np:NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance a np:Provenance .
  dgn-np:NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_assertion {
   miriam-gene:978 a ncit:C16612 .
  lld:C0023467 a ncit:C7057 .
  dgn-gda:DGN1f9350398eb97cf2c6a0a8252dda1a53 sio:SIO_000628 miriam-gene:978 , lld:C0023467 ;
    a sio:SIO_001121 .
}
dgn-np:NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_provenance {
   dgn-np:NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_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:NP402959.RA6yF94G9ETfw1PuVh9rmP1U7ISnLHKPAxor4zgQYR2UE130_publicationInfo {
   this: dcterms:created "2014-10-02T12:36:00+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" .
}