@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E> .
@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:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_head {
  this: np:hasAssertion dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_assertion;
    np:hasProvenance dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_provenance;
    np:hasPublicationInfo dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_assertion a np:Assertion .
  
  dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_provenance a np:Provenance .
  
  dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_assertion {
  miriam-gene:1543 a ncit:C16612 .
  
  lld:C0546837 a ncit:C7057 .
  
  dgn-gda:DGN0959a2081e2172d6a9dcabb923125bc7 sio:SIO_000628 miriam-gene:1543, lld:C0546837;
    a sio:SIO_001122 .
}

dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_provenance {
  dgn-np:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_assertion dcterms:description
      "[There were no significant differences in the frequency distribution of CYP1A1 polymorphisms between esophageal cancer patients and healthy controls although the frequency of CYP1A1 with at least one allele of Val showed slightly higher in individuals with esophageal cancer.]. 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:11860825;
    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:NP46052.RANen_XXhD_MnDpJBH84WH_cMsVV3VZfdlv10jCCFb8-E130_publicationInfo {
  this: dcterms:created "2014-10-02T12:32:21+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" .
}