@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP265278.RAfrt_-EoExP5ifBgyjSx2tdTwd4oXE2N0DJZk-tNJGPo> .
@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:NP265278.RAfrt_-EoExP5ifBgyjSx2tdTwd4oXE2N0DJZk-tNJGPo130_head {
  this: np:hasAssertion dgn-np:NP265278.RAfrt_-EoExP5ifBgyjSx2tdTwd4oXE2N0DJZk-tNJGPo130_assertion;
    np:hasProvenance dgn-np:NP265278.RAfrt_-EoExP5ifBgyjSx2tdTwd4oXE2N0DJZk-tNJGPo130_provenance;
    np:hasPublicationInfo dgn-np:NP265278.RAfrt_-EoExP5ifBgyjSx2tdTwd4oXE2N0DJZk-tNJGPo130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP265278.RAfrt_-EoExP5ifBgyjSx2tdTwd4oXE2N0DJZk-tNJGPo130_assertion a np:Assertion .
  
  dgn-np:NP265278.RAfrt_-EoExP5ifBgyjSx2tdTwd4oXE2N0DJZk-tNJGPo130_provenance a np:Provenance .
  
  dgn-np:NP265278.RAfrt_-EoExP5ifBgyjSx2tdTwd4oXE2N0DJZk-tNJGPo130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP265278.RAfrt_-EoExP5ifBgyjSx2tdTwd4oXE2N0DJZk-tNJGPo130_assertion {
  miriam-gene:595 a ncit:C16612 .
  
  lld:C0004763 a ncit:C7057 .
  
  dgn-gda:DGN4f423cf00b31fe42bb378d01bc5b0c0c sio:SIO_000628 miriam-gene:595, lld:C0004763;
    a sio:SIO_001121 .
}

dgn-np:NP265278.RAfrt_-EoExP5ifBgyjSx2tdTwd4oXE2N0DJZk-tNJGPo130_provenance {
  dgn-np:NP265278.RAfrt_-EoExP5ifBgyjSx2tdTwd4oXE2N0DJZk-tNJGPo130_assertion dcterms:description
      "[To date, biomarkers which currently appear to predict the progression of Barrett esophagus to invasive malignancy include aneuploidy, loss of heterozygosity of 17p (implicating the p53 tumor suppressor gene), and cyclin D1 protein overexpression, and with further validation, will most likely be incorporated into routine clinical practice.]. 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:16428034;
    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:NP265278.RAfrt_-EoExP5ifBgyjSx2tdTwd4oXE2N0DJZk-tNJGPo130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:28+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" .
}