@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP170932.RA7uezBRaletTVs05uYWkc4BKTczYrNjgdgM0aRjWPMN4> .
@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:NP170932.RA7uezBRaletTVs05uYWkc4BKTczYrNjgdgM0aRjWPMN4130_head {
  this: np:hasAssertion dgn-np:NP170932.RA7uezBRaletTVs05uYWkc4BKTczYrNjgdgM0aRjWPMN4130_assertion ;
    np:hasProvenance dgn-np:NP170932.RA7uezBRaletTVs05uYWkc4BKTczYrNjgdgM0aRjWPMN4130_provenance ;
    np:hasPublicationInfo dgn-np:NP170932.RA7uezBRaletTVs05uYWkc4BKTczYrNjgdgM0aRjWPMN4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP170932.RA7uezBRaletTVs05uYWkc4BKTczYrNjgdgM0aRjWPMN4130_assertion a np:Assertion .
  dgn-np:NP170932.RA7uezBRaletTVs05uYWkc4BKTczYrNjgdgM0aRjWPMN4130_provenance a np:Provenance .
  dgn-np:NP170932.RA7uezBRaletTVs05uYWkc4BKTczYrNjgdgM0aRjWPMN4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP170932.RA7uezBRaletTVs05uYWkc4BKTczYrNjgdgM0aRjWPMN4130_assertion {
  miriam-gene:27102 a ncit:C16612 .
  lld:C0085390 a ncit:C7057 .
  dgn-gda:DGN2d667e260e019b8a577879ec3e94114b sio:SIO_000628 miriam-gene:27102 , lld:C0085390 ;
    a sio:SIO_001121 .
}
dgn-np:NP170932.RA7uezBRaletTVs05uYWkc4BKTczYrNjgdgM0aRjWPMN4130_provenance {
  dgn-np:NP170932.RA7uezBRaletTVs05uYWkc4BKTczYrNjgdgM0aRjWPMN4130_assertion dcterms:description "[In order to examine further the requirement for p53 in HSER and UVER, we have examined host cell reactivation (HCR) of the reporter construct in HS treated, UV treated and mock treated Li-Fraumeni syndrome (LFS) fibroblasts, which are heterozygous for a p53 mutation, and immortalized LFS cell sublines, which express only mutant p53.]. 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:9054614 ;
    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:NP170932.RA7uezBRaletTVs05uYWkc4BKTczYrNjgdgM0aRjWPMN4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:32+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" .
}