@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY> .
@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:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_head {
  this: np:hasAssertion dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_assertion;
    np:hasProvenance dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_provenance;
    np:hasPublicationInfo dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_assertion a np:Assertion .
  
  dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_provenance a np:Provenance .
  
  dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_assertion {
  miriam-gene:133482 a ncit:C16612 .
  
  lld:C0007115 a ncit:C7057 .
  
  dgn-gda:DGN49c5886d89dc8864c5412caa4670ec7f sio:SIO_000628 miriam-gene:133482, lld:C0007115;
    a sio:SIO_001121 .
}

dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_provenance {
  dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_assertion dcterms:description
      "[Nevertheless, as far as we know, only few studies have been conducted linking thyroid cancer incidence and GST polymorphisms, and no data are available on the possible association between NAT2 polymorphisms and thyroid cancer risk.]. 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:19169061;
    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:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:41+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" .
}