@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg> .
@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:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_head {
  this: np:hasAssertion dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_assertion;
    np:hasProvenance dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_provenance;
    np:hasPublicationInfo dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_assertion a np:Assertion .
  
  dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_provenance a np:Provenance .
  
  dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C0877373 a ncit:C7057 .
  
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dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_provenance {
  dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_assertion dcterms:description
      "[One of the main reasons why most patients with advanced cancer are not curable with the therapies available is the broad heterogeneity of cancer cells, inherently related to their genomic instability that reflects defects of cell cycle checkpoints and DNA mismatch repair (MMR).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
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    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:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:23+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>,
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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" .
}