@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP373148.RAf8wpiLHdRpkskhfpto5aaMrvSSmd2CoHJ9hGfKyui1c> .
@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:NP373148.RAf8wpiLHdRpkskhfpto5aaMrvSSmd2CoHJ9hGfKyui1c130_head {
  this: np:hasAssertion dgn-np:NP373148.RAf8wpiLHdRpkskhfpto5aaMrvSSmd2CoHJ9hGfKyui1c130_assertion;
    np:hasProvenance dgn-np:NP373148.RAf8wpiLHdRpkskhfpto5aaMrvSSmd2CoHJ9hGfKyui1c130_provenance;
    np:hasPublicationInfo dgn-np:NP373148.RAf8wpiLHdRpkskhfpto5aaMrvSSmd2CoHJ9hGfKyui1c130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP373148.RAf8wpiLHdRpkskhfpto5aaMrvSSmd2CoHJ9hGfKyui1c130_assertion a np:Assertion .
  
  dgn-np:NP373148.RAf8wpiLHdRpkskhfpto5aaMrvSSmd2CoHJ9hGfKyui1c130_provenance a np:Provenance .
  
  dgn-np:NP373148.RAf8wpiLHdRpkskhfpto5aaMrvSSmd2CoHJ9hGfKyui1c130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP373148.RAf8wpiLHdRpkskhfpto5aaMrvSSmd2CoHJ9hGfKyui1c130_assertion {
  miriam-gene:2944 a ncit:C16612 .
  
  lld:C0085409 a ncit:C7057 .
  
  dgn-gda:DGN10f463e658b6ca9cc2407d429b7f53c3 sio:SIO_000628 miriam-gene:2944, lld:C0085409;
    a sio:SIO_001121 .
}

dgn-np:NP373148.RAf8wpiLHdRpkskhfpto5aaMrvSSmd2CoHJ9hGfKyui1c130_provenance {
  dgn-np:NP373148.RAf8wpiLHdRpkskhfpto5aaMrvSSmd2CoHJ9hGfKyui1c130_assertion dcterms:description
      "[In the selected population the urinary styrene metabolites mandelic (MA) and phenylglyoxylic (PGA) acids were quantified, sister chromatid exchanges (SCE) and micronuclei (MN) were assessed in peripheral lymphocytes and all the subjects were genotyped for GSTM1, GSTT1 (gene deletions), GSTP1 (codon 105 ile==>val), EPHX1 (codons 113 tyr==>his and 139 his==>arg) and CYP2E1 (DraI polymorphism in intron 6).]. 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:14751678;
    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:NP373148.RAf8wpiLHdRpkskhfpto5aaMrvSSmd2CoHJ9hGfKyui1c130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:38+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" .
}