@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP977461.RAXR9bXyAnJdtNMotQvw-714PLgs8GGrCdd-K61x2lWOk> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP977461.RAXR9bXyAnJdtNMotQvw-714PLgs8GGrCdd-K61x2lWOk130_head {
  this: np:hasAssertion dgn-np:NP977461.RAXR9bXyAnJdtNMotQvw-714PLgs8GGrCdd-K61x2lWOk130_assertion;
    np:hasProvenance dgn-np:NP977461.RAXR9bXyAnJdtNMotQvw-714PLgs8GGrCdd-K61x2lWOk130_provenance;
    np:hasPublicationInfo dgn-np:NP977461.RAXR9bXyAnJdtNMotQvw-714PLgs8GGrCdd-K61x2lWOk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP977461.RAXR9bXyAnJdtNMotQvw-714PLgs8GGrCdd-K61x2lWOk130_assertion a np:Assertion .
  
  dgn-np:NP977461.RAXR9bXyAnJdtNMotQvw-714PLgs8GGrCdd-K61x2lWOk130_provenance a np:Provenance .
  
  dgn-np:NP977461.RAXR9bXyAnJdtNMotQvw-714PLgs8GGrCdd-K61x2lWOk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP977461.RAXR9bXyAnJdtNMotQvw-714PLgs8GGrCdd-K61x2lWOk130_assertion {
  miriam-gene:164045 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGNe9a25dda43b390c69481d85fd77cb407 sio:SIO_000628 miriam-gene:164045, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP977461.RAXR9bXyAnJdtNMotQvw-714PLgs8GGrCdd-K61x2lWOk130_provenance {
  dgn-np:NP977461.RAXR9bXyAnJdtNMotQvw-714PLgs8GGrCdd-K61x2lWOk130_assertion dcterms:description
      "[Mutations of the human RecQ helicase genes WRN and BLM lead to rare autosomal recessive disorders, Werner and Bloom syndromes, which are associated with premature aging and cancer predisposition, including breast cancer.]. 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:19205873;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP977461.RAXR9bXyAnJdtNMotQvw-714PLgs8GGrCdd-K61x2lWOk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:47:37+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}