@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP299787.RAetmJo80IyJNppROxRSoQSPeWE7zwdDTZ8e79DbZ_FFQ> .
@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:NP299787.RAetmJo80IyJNppROxRSoQSPeWE7zwdDTZ8e79DbZ_FFQ130_head {
  this: np:hasAssertion dgn-np:NP299787.RAetmJo80IyJNppROxRSoQSPeWE7zwdDTZ8e79DbZ_FFQ130_assertion;
    np:hasProvenance dgn-np:NP299787.RAetmJo80IyJNppROxRSoQSPeWE7zwdDTZ8e79DbZ_FFQ130_provenance;
    np:hasPublicationInfo dgn-np:NP299787.RAetmJo80IyJNppROxRSoQSPeWE7zwdDTZ8e79DbZ_FFQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP299787.RAetmJo80IyJNppROxRSoQSPeWE7zwdDTZ8e79DbZ_FFQ130_assertion a np:Assertion .
  
  dgn-np:NP299787.RAetmJo80IyJNppROxRSoQSPeWE7zwdDTZ8e79DbZ_FFQ130_provenance a np:Provenance .
  
  dgn-np:NP299787.RAetmJo80IyJNppROxRSoQSPeWE7zwdDTZ8e79DbZ_FFQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP299787.RAetmJo80IyJNppROxRSoQSPeWE7zwdDTZ8e79DbZ_FFQ130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0751688 a ncit:C7057 .
  
  dgn-gda:DGN185ff3673f7267855256feec2ec97d0a sio:SIO_000628 miriam-gene:7157, lld:C0751688;
    a sio:SIO_001121 .
}

dgn-np:NP299787.RAetmJo80IyJNppROxRSoQSPeWE7zwdDTZ8e79DbZ_FFQ130_provenance {
  dgn-np:NP299787.RAetmJo80IyJNppROxRSoQSPeWE7zwdDTZ8e79DbZ_FFQ130_assertion dcterms:description
      "[This was achieved through the retroviral-mediated transduction into normal, primary human esophageal epithelial cells of epidermal growth factor receptor (EGFR), the catalytic subunit of human telomerase (hTERT), and p53(R175H), genes that are frequently altered in human esophageal squamous cell 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:17974918;
    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:NP299787.RAetmJo80IyJNppROxRSoQSPeWE7zwdDTZ8e79DbZ_FFQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:50+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" .
}