@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP177100.RARQXW1-8KX-aROcal3XOFl9KfP-d6cEnuI1CqA9K0gQU> .
@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:NP177100.RARQXW1-8KX-aROcal3XOFl9KfP-d6cEnuI1CqA9K0gQU130_head {
  this: np:hasAssertion dgn-np:NP177100.RARQXW1-8KX-aROcal3XOFl9KfP-d6cEnuI1CqA9K0gQU130_assertion;
    np:hasProvenance dgn-np:NP177100.RARQXW1-8KX-aROcal3XOFl9KfP-d6cEnuI1CqA9K0gQU130_provenance;
    np:hasPublicationInfo dgn-np:NP177100.RARQXW1-8KX-aROcal3XOFl9KfP-d6cEnuI1CqA9K0gQU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP177100.RARQXW1-8KX-aROcal3XOFl9KfP-d6cEnuI1CqA9K0gQU130_assertion a np:Assertion .
  
  dgn-np:NP177100.RARQXW1-8KX-aROcal3XOFl9KfP-d6cEnuI1CqA9K0gQU130_provenance a np:Provenance .
  
  dgn-np:NP177100.RARQXW1-8KX-aROcal3XOFl9KfP-d6cEnuI1CqA9K0gQU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP177100.RARQXW1-8KX-aROcal3XOFl9KfP-d6cEnuI1CqA9K0gQU130_assertion {
  miriam-gene:7157 a ncit:C16612 .
  
  lld:C0006079 a ncit:C7057 .
  
  dgn-gda:DGN09f442529335728a2191ed08351487aa sio:SIO_000628 miriam-gene:7157, lld:C0006079;
    a sio:SIO_001121 .
}

dgn-np:NP177100.RARQXW1-8KX-aROcal3XOFl9KfP-d6cEnuI1CqA9K0gQU130_provenance {
  dgn-np:NP177100.RARQXW1-8KX-aROcal3XOFl9KfP-d6cEnuI1CqA9K0gQU130_assertion dcterms:description
      "[To examine the contribution of environmental or endogenous mutagens other than UVR, which are expected to be relatively more important to the overall burden of NMSCs in the Japanese, we directly sequenced exons 5-8 of the p53 tumour suppressor gene in 29 Japanese patients with Bowen's disease, an in situ squamous-cell carcinoma of the skin.]. 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:9139870;
    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:NP177100.RARQXW1-8KX-aROcal3XOFl9KfP-d6cEnuI1CqA9K0gQU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:35+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" .
}