@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP58833.RAIJR7sD8d_uES66Hf5_ypw4fTsWHljw_3cvruN55aaQA> .
@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:NP58833.RAIJR7sD8d_uES66Hf5_ypw4fTsWHljw_3cvruN55aaQA130_head {
   this: np:hasAssertion dgn-np:NP58833.RAIJR7sD8d_uES66Hf5_ypw4fTsWHljw_3cvruN55aaQA130_assertion ;
    np:hasProvenance dgn-np:NP58833.RAIJR7sD8d_uES66Hf5_ypw4fTsWHljw_3cvruN55aaQA130_provenance ;
    np:hasPublicationInfo dgn-np:NP58833.RAIJR7sD8d_uES66Hf5_ypw4fTsWHljw_3cvruN55aaQA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP58833.RAIJR7sD8d_uES66Hf5_ypw4fTsWHljw_3cvruN55aaQA130_assertion a np:Assertion .
  dgn-np:NP58833.RAIJR7sD8d_uES66Hf5_ypw4fTsWHljw_3cvruN55aaQA130_provenance a np:Provenance .
  dgn-np:NP58833.RAIJR7sD8d_uES66Hf5_ypw4fTsWHljw_3cvruN55aaQA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP58833.RAIJR7sD8d_uES66Hf5_ypw4fTsWHljw_3cvruN55aaQA130_assertion {
   miriam-gene:7172 a ncit:C16612 .
  lld:C0023418 a ncit:C7057 .
  dgn-gda:DGNa55613b8cfad0035b593658adea871cd sio:SIO_000628 miriam-gene:7172 , lld:C0023418 ;
    a sio:SIO_001122 .
}
dgn-np:NP58833.RAIJR7sD8d_uES66Hf5_ypw4fTsWHljw_3cvruN55aaQA130_provenance {
   dgn-np:NP58833.RAIJR7sD8d_uES66Hf5_ypw4fTsWHljw_3cvruN55aaQA130_assertion dcterms:description "[To investigate the allelic frequencies and distribution of single-nucleotide polymorphisms within the coding region (cSNPs) of thiopurine S-methyltransferase gene (TPMT) in Chinese children with acute leukemia (AL) and healthy controls, in order to provide genetic references for individual chemotherapy for AL patients by studying the relationship between the cSNP in human TPMT and chemotherapeutic effect of thiopurine drugs.]. 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:20017316 ;
    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:NP58833.RAIJR7sD8d_uES66Hf5_ypw4fTsWHljw_3cvruN55aaQA130_publicationInfo {
   this: dcterms:created "2014-10-02T12:32:27+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" .
}