@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ> .
@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:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_head {
  this: np:hasAssertion dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_assertion;
    np:hasProvenance dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_provenance;
    np:hasPublicationInfo dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_assertion a np:Assertion .
  
  dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_provenance a np:Provenance .
  
  dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C1332347 a ncit:C7057 .
  
  dgn-gda:DGN5dc344605200c2c07fd26371d476db45 sio:SIO_000628 miriam-gene:7157, lld:C1332347;
    a sio:SIO_001121 .
}

dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_provenance {
  dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_assertion dcterms:description
      "[The aims of this study were to determine the status and timing of p53 mutation in the progression from atypical ductal hyperplasia to invasive cancer, and to evaluate the patterns of p53 mutations in noninvasive and invasive lesions.]. 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:11715068;
    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:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:40+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" .
}