@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP304924.RAeoafbOxOusPieSlEikjf1zkCu40Acsm1IGUKUp9URwA> .
@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:NP304924.RAeoafbOxOusPieSlEikjf1zkCu40Acsm1IGUKUp9URwA130_head {
  this: np:hasAssertion dgn-np:NP304924.RAeoafbOxOusPieSlEikjf1zkCu40Acsm1IGUKUp9URwA130_assertion ;
    np:hasProvenance dgn-np:NP304924.RAeoafbOxOusPieSlEikjf1zkCu40Acsm1IGUKUp9URwA130_provenance ;
    np:hasPublicationInfo dgn-np:NP304924.RAeoafbOxOusPieSlEikjf1zkCu40Acsm1IGUKUp9URwA130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP304924.RAeoafbOxOusPieSlEikjf1zkCu40Acsm1IGUKUp9URwA130_assertion a np:Assertion .
  dgn-np:NP304924.RAeoafbOxOusPieSlEikjf1zkCu40Acsm1IGUKUp9URwA130_provenance a np:Provenance .
  dgn-np:NP304924.RAeoafbOxOusPieSlEikjf1zkCu40Acsm1IGUKUp9URwA130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP304924.RAeoafbOxOusPieSlEikjf1zkCu40Acsm1IGUKUp9URwA130_assertion {
  miriam-gene:7157 a ncit:C16612 .
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    a sio:SIO_001121 .
}
dgn-np:NP304924.RAeoafbOxOusPieSlEikjf1zkCu40Acsm1IGUKUp9URwA130_provenance {
  dgn-np:NP304924.RAeoafbOxOusPieSlEikjf1zkCu40Acsm1IGUKUp9URwA130_assertion dcterms:description "[Our observations indicate that mutations of the p53 gene are not the major molecular etiology for porokeratosis, but are related to its skin carcinogenesis, and that p53 overexpression in porokeratosis is not due to p53 gene mutations.]. 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:9138474 ;
    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:NP304924.RAeoafbOxOusPieSlEikjf1zkCu40Acsm1IGUKUp9URwA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:55+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 ;
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    pav:createdBy <http://orcid.org/0000-0003-0169-8159> ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}