@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM> .
@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:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_head {
  this: np:hasAssertion dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_assertion;
    np:hasProvenance dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_provenance;
    np:hasPublicationInfo dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_assertion a np:Assertion .
  
  dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_provenance a np:Provenance .
  
  dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_assertion {
  miriam-gene:1029 a ncit:C16612 .
  
  lld:C0079474 a ncit:C7057 .
  
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    a sio:SIO_001121 .
}

dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_provenance {
  dgn-np:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_assertion dcterms:description
      "[This is the first description of specific abnormalities in tumor suppressor genes in RDEB associated SCC, and demonstrates that alterations in both p53 and p16ink4a can contribute to RDEB associated SCC.]. 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:15373786;
    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:NP881990.RAf5amri93czwQj9zBBUEfSKujtMUd1-AW16sjPIo3DUM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:59+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" .
}