@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP424372.RAMLfWhG3O2FjKi2D8m2VAQWs6rrW89OpS0ZYJrJO1lZU> .
@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:NP424372.RAMLfWhG3O2FjKi2D8m2VAQWs6rrW89OpS0ZYJrJO1lZU130_head {
  this: np:hasAssertion dgn-np:NP424372.RAMLfWhG3O2FjKi2D8m2VAQWs6rrW89OpS0ZYJrJO1lZU130_assertion;
    np:hasProvenance dgn-np:NP424372.RAMLfWhG3O2FjKi2D8m2VAQWs6rrW89OpS0ZYJrJO1lZU130_provenance;
    np:hasPublicationInfo dgn-np:NP424372.RAMLfWhG3O2FjKi2D8m2VAQWs6rrW89OpS0ZYJrJO1lZU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP424372.RAMLfWhG3O2FjKi2D8m2VAQWs6rrW89OpS0ZYJrJO1lZU130_assertion a np:Assertion .
  
  dgn-np:NP424372.RAMLfWhG3O2FjKi2D8m2VAQWs6rrW89OpS0ZYJrJO1lZU130_provenance a np:Provenance .
  
  dgn-np:NP424372.RAMLfWhG3O2FjKi2D8m2VAQWs6rrW89OpS0ZYJrJO1lZU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP424372.RAMLfWhG3O2FjKi2D8m2VAQWs6rrW89OpS0ZYJrJO1lZU130_assertion {
  miriam-gene:9401 a ncit:C16612 .
  
  lld:C0231341 a ncit:C7057 .
  
  dgn-gda:DGNade4658f1185368d98c43f9282ac7125 sio:SIO_000628 miriam-gene:9401, lld:C0231341;
    a sio:SIO_001121 .
}

dgn-np:NP424372.RAMLfWhG3O2FjKi2D8m2VAQWs6rrW89OpS0ZYJrJO1lZU130_provenance {
  dgn-np:NP424372.RAMLfWhG3O2FjKi2D8m2VAQWs6rrW89OpS0ZYJrJO1lZU130_assertion dcterms:description
      "[Genetic defects in three of the five human RecQ helicases, BLM, WRN and RECQ4, give rise to defined syndromes associated with cancer predisposition, some features of premature ageing and chromosomal instability.]. 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:19657341;
    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:NP424372.RAMLfWhG3O2FjKi2D8m2VAQWs6rrW89OpS0ZYJrJO1lZU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:12+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" .
}