@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP426547.RADXm3dEVuAFqRxOIK2NABKGZyQfSaPk2Sit6EoVoGROc> .
@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:NP426547.RADXm3dEVuAFqRxOIK2NABKGZyQfSaPk2Sit6EoVoGROc130_head {
  this: np:hasAssertion dgn-np:NP426547.RADXm3dEVuAFqRxOIK2NABKGZyQfSaPk2Sit6EoVoGROc130_assertion;
    np:hasProvenance dgn-np:NP426547.RADXm3dEVuAFqRxOIK2NABKGZyQfSaPk2Sit6EoVoGROc130_provenance;
    np:hasPublicationInfo dgn-np:NP426547.RADXm3dEVuAFqRxOIK2NABKGZyQfSaPk2Sit6EoVoGROc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP426547.RADXm3dEVuAFqRxOIK2NABKGZyQfSaPk2Sit6EoVoGROc130_assertion a np:Assertion .
  
  dgn-np:NP426547.RADXm3dEVuAFqRxOIK2NABKGZyQfSaPk2Sit6EoVoGROc130_provenance a np:Provenance .
  
  dgn-np:NP426547.RADXm3dEVuAFqRxOIK2NABKGZyQfSaPk2Sit6EoVoGROc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP426547.RADXm3dEVuAFqRxOIK2NABKGZyQfSaPk2Sit6EoVoGROc130_assertion {
  miriam-gene:7248 a ncit:C16612 .
  
  lld:C0206698 a ncit:C7057 .
  
  dgn-gda:DGNa8a7a7b4bdc4d7e6d0b930467f513cba sio:SIO_000628 miriam-gene:7248, lld:C0206698;
    a sio:SIO_001121 .
}

dgn-np:NP426547.RADXm3dEVuAFqRxOIK2NABKGZyQfSaPk2Sit6EoVoGROc130_provenance {
  dgn-np:NP426547.RADXm3dEVuAFqRxOIK2NABKGZyQfSaPk2Sit6EoVoGROc130_assertion dcterms:description
      "[Inactivation of the tumour suppressor gene p53, is the commonest genetic abnormality in human cancer and has been implicated in the genesis of cholangiocarcinoma in various immunohistochemical and molecular epidemiological investigations, including gene sequencing studies.]. 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:15998419;
    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:NP426547.RADXm3dEVuAFqRxOIK2NABKGZyQfSaPk2Sit6EoVoGROc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:13+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" .
}