@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP318805.RAc6pNufSZp5CJZgeVt0kModl1sN3GXQ3JVSl4kMtEg1w> .
@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:NP318805.RAc6pNufSZp5CJZgeVt0kModl1sN3GXQ3JVSl4kMtEg1w130_head {
  this: np:hasAssertion dgn-np:NP318805.RAc6pNufSZp5CJZgeVt0kModl1sN3GXQ3JVSl4kMtEg1w130_assertion;
    np:hasProvenance dgn-np:NP318805.RAc6pNufSZp5CJZgeVt0kModl1sN3GXQ3JVSl4kMtEg1w130_provenance;
    np:hasPublicationInfo dgn-np:NP318805.RAc6pNufSZp5CJZgeVt0kModl1sN3GXQ3JVSl4kMtEg1w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP318805.RAc6pNufSZp5CJZgeVt0kModl1sN3GXQ3JVSl4kMtEg1w130_assertion a np:Assertion .
  
  dgn-np:NP318805.RAc6pNufSZp5CJZgeVt0kModl1sN3GXQ3JVSl4kMtEg1w130_provenance a np:Provenance .
  
  dgn-np:NP318805.RAc6pNufSZp5CJZgeVt0kModl1sN3GXQ3JVSl4kMtEg1w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP318805.RAc6pNufSZp5CJZgeVt0kModl1sN3GXQ3JVSl4kMtEg1w130_assertion {
  miriam-gene:7422 a ncit:C16612 .
  
  lld:C0152018 a ncit:C7057 .
  
  dgn-gda:DGNc2eacc703731c1aa29ae7a010f7f6ecd sio:SIO_000628 miriam-gene:7422, lld:C0152018;
    a sio:SIO_001121 .
}

dgn-np:NP318805.RAc6pNufSZp5CJZgeVt0kModl1sN3GXQ3JVSl4kMtEg1w130_provenance {
  dgn-np:NP318805.RAc6pNufSZp5CJZgeVt0kModl1sN3GXQ3JVSl4kMtEg1w130_assertion dcterms:description
      "[Although the mechanism on the induction of VEGF gene is still unclear in human cancer tissue, we obtained the informative evidence indicating that p53 mutation is involved in VEGF expression of 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:10457902;
    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:NP318805.RAc6pNufSZp5CJZgeVt0kModl1sN3GXQ3JVSl4kMtEg1w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:05+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" .
}