@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP182022.RADHezaXkH7RwKU7tvCI0iLpzK4y9tmRjV7udCvYFZ3jo> .
@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:NP182022.RADHezaXkH7RwKU7tvCI0iLpzK4y9tmRjV7udCvYFZ3jo130_head {
  this: np:hasAssertion dgn-np:NP182022.RADHezaXkH7RwKU7tvCI0iLpzK4y9tmRjV7udCvYFZ3jo130_assertion;
    np:hasProvenance dgn-np:NP182022.RADHezaXkH7RwKU7tvCI0iLpzK4y9tmRjV7udCvYFZ3jo130_provenance;
    np:hasPublicationInfo dgn-np:NP182022.RADHezaXkH7RwKU7tvCI0iLpzK4y9tmRjV7udCvYFZ3jo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP182022.RADHezaXkH7RwKU7tvCI0iLpzK4y9tmRjV7udCvYFZ3jo130_assertion a np:Assertion .
  
  dgn-np:NP182022.RADHezaXkH7RwKU7tvCI0iLpzK4y9tmRjV7udCvYFZ3jo130_provenance a np:Provenance .
  
  dgn-np:NP182022.RADHezaXkH7RwKU7tvCI0iLpzK4y9tmRjV7udCvYFZ3jo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP182022.RADHezaXkH7RwKU7tvCI0iLpzK4y9tmRjV7udCvYFZ3jo130_assertion {
  miriam-gene:27306 a ncit:C16612 .
  
  lld:C0206708 a ncit:C7057 .
  
  dgn-gda:DGNfec318f4c0f0dd2e61aa8ff1fcbf519e sio:SIO_000628 miriam-gene:27306, lld:C0206708;
    a sio:SIO_001121 .
}

dgn-np:NP182022.RADHezaXkH7RwKU7tvCI0iLpzK4y9tmRjV7udCvYFZ3jo130_provenance {
  dgn-np:NP182022.RADHezaXkH7RwKU7tvCI0iLpzK4y9tmRjV7udCvYFZ3jo130_assertion dcterms:description
      "[In this investigation, we explored the hypothesis that genetic polymorphisms in the cytochrome P4501A1 (T3801C) and glutathione S-transferase classes mu and theta (GSTM1 and GSTT1) gene deletions promote the development of cervical dysplasia by moderating the activation and detoxification of polycyclic hydrocarbons and other compounds that influence oxidative stress and DNA adduct formation.]. 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:11330960;
    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:NP182022.RADHezaXkH7RwKU7tvCI0iLpzK4y9tmRjV7udCvYFZ3jo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:38+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" .
}