@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8> .
@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:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_head {
  this: np:hasAssertion dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_assertion;
    np:hasProvenance dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_provenance;
    np:hasPublicationInfo dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_assertion a np:Assertion .
  
  dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_provenance a np:Provenance .
  
  dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_assertion {
  miriam-gene:641 a ncit:C16612 .
  
  lld:C0231341 a ncit:C7057 .
  
  dgn-gda:DGN034eacb8dcd81b6d7ab5895779d54422 sio:SIO_000628 miriam-gene:641, lld:C0231341;
    a sio:SIO_001121 .
}

dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_provenance {
  dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_assertion dcterms:description
      "[Human cells defective in a different RecQ helicase, the WRN protein involved in the premature aging Werner syndrome, do not exhibit the gene cluster instability (GCI) phenotype, indicating that the BLM protein specifically, rather than RecQ helicases generally, holds back this recombination-mediated genomic 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:19542097;
    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:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:43+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" .
}