@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk> .
@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:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_head {
  this: np:hasAssertion dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_assertion;
    np:hasProvenance dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_provenance;
    np:hasPublicationInfo dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_assertion a np:Assertion .
  
  dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_provenance a np:Provenance .
  
  dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0032927 a ncit:C7057 .
  
  dgn-gda:DGN0415356fd108fff5f56a3005c86f980c sio:SIO_000628 miriam-gene:1029, lld:C0032927;
    a sio:SIO_001121 .
}

dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_provenance {
  dgn-np:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_assertion dcterms:description
      "[The aim of this study was to characterize the spectrum of p16 alterations in surgically resected esophageal tissues, comprising histologically normal esophageal squamous and gastric epithelia, premalignant Barrett's epithelia, and associated esophageal adenocarcinomas, and to explore associations between p16 mRNA expression and p16 mutations, deletions, promoter hypermethylation, p16 protein expression, and clinico-pathologic features for the same tissues.]. 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:15617840;
    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:NP190788.RAc7gEkC3x908c4Om5DjTlLdDQCLCfjXS1i7x0rNNS-Qk130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:45+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" .
}