@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_head {
  this: np:hasAssertion dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_assertion;
    np:hasProvenance dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_provenance;
    np:hasPublicationInfo dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_assertion a np:Assertion .
  
  dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_provenance a np:Provenance .
  
  dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_assertion {
  miriam-gene:5111 a ncit:C16612 .
  
  lld:C0279626 a ncit:C7057 .
  
  dgn-gda:DGN1ec65ee15c13f2c29c21a76ee4348e78 sio:SIO_000628 miriam-gene:5111, lld:C0279626;
    a sio:SIO_001121 .
}

dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_provenance {
  dgn-np:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_assertion dcterms:description
      "[The high coincident alterations for P53 and PCNA in SCC and GCA from the same patient indicate the possibility of similar molecular basis, which provides important molecular basis and etiological clue for similar geographic distribution and risk factors in SCC and GCA.]. 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:12508343;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP612035.RAhfp7k5Nb3YQHeifDUgpG2knDIhfcwt329hEe88I6fzk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:46+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}