@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck> .
@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:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_head {
  this: np:hasAssertion dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_assertion;
    np:hasProvenance dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_provenance;
    np:hasPublicationInfo dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_assertion a np:Assertion .
  
  dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_provenance a np:Provenance .
  
  dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_assertion {
  miriam-gene:3251 a ncit:C16612 .
  
  lld:C1140680 a ncit:C7057 .
  
  dgn-gda:DGN19e0e9b532b70e89f1c02c7bf3347af3 sio:SIO_000628 miriam-gene:3251, lld:C1140680;
    a sio:SIO_001121 .
}

dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_provenance {
  dgn-np:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_assertion dcterms:description
      "[We demonstrated that, in a limited number of colonies from an ovarian cancer, there was an ability to increase the mutation frequency at the HPRT locus after exposure to common chemotheraputics used in the treatment of this disease.]. 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:16158952;
    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:NP485263.RAAx_VGCnLYmr2AwPM8wsMbbgkbala3SsBEsZy5isW9ck130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:50+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" .
}