@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_head {
  this: np:hasAssertion dgn-np:NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_assertion;
    np:hasProvenance dgn-np:NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance;
    np:hasPublicationInfo dgn-np:NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_assertion a np:Assertion .
  
  dgn-np:NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance a np:Provenance .
  
  dgn-np:NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_assertion {
  miriam-gene:1545 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNb0d7eff9d458a3c6c23506f5ac49f100 sio:SIO_000628 miriam-gene:1545, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_provenance {
  dgn-np:NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_assertion dcterms:description
      "[However, the specific combination of GSTM1 null, GSTT1 null, and CYP1B1 codon 119 risk allele carriers and specific combination of GSTM1 present, GSTT1 null, and CYP1B1 432 risk allele carriers exhibited increased cancer risk in the combined analysis.]. 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:23886208;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP340188.RASyuL_o_4YE9TQRn7vV-3Lj0bTU6_sJWUPaef-F22SpE130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:56+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}