@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1347180.RAr01l-lwly4TfNw7v520qNYqnr430uxjO_XgKH6JZwVQ> .
@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/v4.0.0/void/> .

dgn-np:NP1347180.RAr01l-lwly4TfNw7v520qNYqnr430uxjO_XgKH6JZwVQ130_head {
  this: np:hasAssertion dgn-np:NP1347180.RAr01l-lwly4TfNw7v520qNYqnr430uxjO_XgKH6JZwVQ130_assertion;
    np:hasProvenance dgn-np:NP1347180.RAr01l-lwly4TfNw7v520qNYqnr430uxjO_XgKH6JZwVQ130_provenance;
    np:hasPublicationInfo dgn-np:NP1347180.RAr01l-lwly4TfNw7v520qNYqnr430uxjO_XgKH6JZwVQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1347180.RAr01l-lwly4TfNw7v520qNYqnr430uxjO_XgKH6JZwVQ130_assertion a np:Assertion .
  
  dgn-np:NP1347180.RAr01l-lwly4TfNw7v520qNYqnr430uxjO_XgKH6JZwVQ130_provenance a np:Provenance .
  
  dgn-np:NP1347180.RAr01l-lwly4TfNw7v520qNYqnr430uxjO_XgKH6JZwVQ130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1347180.RAr01l-lwly4TfNw7v520qNYqnr430uxjO_XgKH6JZwVQ130_assertion {
  miriam-gene:6530 a ncit:C16612 .
  
  lld:C0005684 a ncit:C7057 .
  
  dgn-gda:DGN3c7842889d30b9103c939b418962475f sio:SIO_000628 miriam-gene:6530, lld:C0005684;
    a sio:SIO_001121 .
}

dgn-np:NP1347180.RAr01l-lwly4TfNw7v520qNYqnr430uxjO_XgKH6JZwVQ130_provenance {
  dgn-np:NP1347180.RAr01l-lwly4TfNw7v520qNYqnr430uxjO_XgKH6JZwVQ130_assertion dcterms:description
      "[In collaborative studies, we now have found that NAT1 is also expressed polymorphically in human bladder due to mutations in the NAT1 polyadenylation signal, which has recently been associated with increased bladder 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:8597119;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP1347180.RAr01l-lwly4TfNw7v520qNYqnr430uxjO_XgKH6JZwVQ130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:57+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}