@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84> .
@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:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_head {
  this: np:hasAssertion dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_assertion;
    np:hasProvenance dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_provenance;
    np:hasPublicationInfo dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_assertion a np:Assertion .
  
  dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_provenance a np:Provenance .
  
  dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C1332922 a ncit:C7057 .
  
  dgn-gda:DGN7f97e85f632244fe8b0d774f7303cc5b sio:SIO_000628 miriam-gene:7157, lld:C1332922;
    a sio:SIO_001121 .
}

dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_provenance {
  dgn-np:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_assertion dcterms:description
      "[These results suggest that inactivation of p53 may allow lung cancer cells to go through an inappropriate second division cycle under certain forms of mitotic stresses, which would result in the induction of the CIN phenotype in conjunction with the generation of aneuploidy.]. 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:11583962;
    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:NP744896.RAw4CAmcgOyn5eOrzmNVpWVXnEg8B2v9jTwgCMD7WkZ84130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:31+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" .
}