@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP709632.RA5vhiAUMV2nDHRsCg1yOCb4BuUn3Zv5KG_CN9oxaiK6k> .
@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:NP709632.RA5vhiAUMV2nDHRsCg1yOCb4BuUn3Zv5KG_CN9oxaiK6k130_head {
  this: np:hasAssertion dgn-np:NP709632.RA5vhiAUMV2nDHRsCg1yOCb4BuUn3Zv5KG_CN9oxaiK6k130_assertion ;
    np:hasProvenance dgn-np:NP709632.RA5vhiAUMV2nDHRsCg1yOCb4BuUn3Zv5KG_CN9oxaiK6k130_provenance ;
    np:hasPublicationInfo dgn-np:NP709632.RA5vhiAUMV2nDHRsCg1yOCb4BuUn3Zv5KG_CN9oxaiK6k130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP709632.RA5vhiAUMV2nDHRsCg1yOCb4BuUn3Zv5KG_CN9oxaiK6k130_assertion a np:Assertion .
  dgn-np:NP709632.RA5vhiAUMV2nDHRsCg1yOCb4BuUn3Zv5KG_CN9oxaiK6k130_provenance a np:Provenance .
  dgn-np:NP709632.RA5vhiAUMV2nDHRsCg1yOCb4BuUn3Zv5KG_CN9oxaiK6k130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP709632.RA5vhiAUMV2nDHRsCg1yOCb4BuUn3Zv5KG_CN9oxaiK6k130_assertion {
  miriam-gene:5111 a ncit:C16612 .
  lld:C0162839 a ncit:C7057 .
  dgn-gda:DGNed9a57cee4a25db4e754cdfc6bc7edc0 sio:SIO_000628 miriam-gene:5111 , lld:C0162839 ;
    a sio:SIO_001121 .
}
dgn-np:NP709632.RA5vhiAUMV2nDHRsCg1yOCb4BuUn3Zv5KG_CN9oxaiK6k130_provenance {
  dgn-np:NP709632.RA5vhiAUMV2nDHRsCg1yOCb4BuUn3Zv5KG_CN9oxaiK6k130_assertion dcterms:description "[The finding of p53 immunoperoxidase staining in porokeratosis suggests genetic mutation, as occurs in other cutaneous keratinocytic neoplasms, and the lack of corresponding proliferating cell nuclear antigen expression in many specimens indicates that p53 overexpression is not simply a reflection of increased cellular proliferation.]. 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:8304757 ;
    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:NP709632.RA5vhiAUMV2nDHRsCg1yOCb4BuUn3Zv5KG_CN9oxaiK6k130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:11+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" .
}