@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc> .
@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:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_head {
  this: np:hasAssertion dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_assertion;
    np:hasProvenance dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_provenance;
    np:hasPublicationInfo dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_assertion a np:Assertion .
  
  dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_provenance a np:Provenance .
  
  dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_assertion {
  miriam-gene:5981 a ncit:C16612 .
  
  lld:C0023418 a ncit:C7057 .
  
  dgn-gda:DGN46c13ab596d6f9bb8e27192f8cdcc949 sio:SIO_000628 miriam-gene:5981, lld:C0023418;
    a sio:SIO_001121 .
}

dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_provenance {
  dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_assertion dcterms:description
      "[The authors devised a genomic polymerase chain reaction-single strand conformational polymorphism assay followed by sequencing and screened the entire RFC coding region for sequence alterations in DNA from 246 leukemia specimens from patients with diverse ethnic variation, 24 at the time of recurrence and the rest at the time of diagnosis.]. 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:14770434;
    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:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:29+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" .
}