@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg> .
@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:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_head {
  this: np:hasAssertion dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_assertion;
    np:hasProvenance dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_provenance;
    np:hasPublicationInfo dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_assertion a np:Assertion .
  
  dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_provenance a np:Provenance .
  
  dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_assertion {
  miriam-gene:1576 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN0cddb791e35c2de138f6d2e90543f864 sio:SIO_000628 miriam-gene:1576, lld:C0006142;
    a sio:SIO_001122 .
}

dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_provenance {
  dgn-np:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_assertion dcterms:description
      "[To characterize pregnane X receptor (PXR) polymorphic variants in healthy Asian populations Chinese, Malay and Indian (n=100 each), and to investigate the association between PXR haplotypes and hepatic mRNA expression of PXR and its downstream target genes, CYP3A4 and ABCB1, as well as their influence on the clearance of doxorubicin in Asian breast cancer patients.]. 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:18981011;
    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:NP60098.RAnvWzFWlkRv7MUEVxrLYt4JfHQXZaKQ4mce7c2ZNvavg130_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" .
}