@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4> .
@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:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_head {
  this: np:hasAssertion dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_assertion;
    np:hasProvenance dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_provenance;
    np:hasPublicationInfo dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_assertion a np:Assertion .
  
  dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_provenance a np:Provenance .
  
  dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_assertion {
  miriam-gene:79947 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN9438c44cb9a3acf98108e2639237aa8f sio:SIO_000628 miriam-gene:79947, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_provenance {
  dgn-np:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_assertion dcterms:description
      "[To determine the differences in DNA damage signalling leading to differential sensitivity to CPT, two human colon cancer cell lines, SW620 and KM12, with nonfunctional p53 and the same level of topoisomerase I cleavable complex formation but differential sensitivity to CPT (Cancer Res.]. 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:8938795;
    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:NP612898.RAbM_JqttJmpWQldsfOZh6nFoqkUtia3rqs1cvU9skNu4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:10+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" .
}