@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP623254.RAvCgZjy9iWCYyiraQ3l9WAvVs1j8ho3LuebLuxOYP3fs> .
@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:NP623254.RAvCgZjy9iWCYyiraQ3l9WAvVs1j8ho3LuebLuxOYP3fs130_head {
  this: np:hasAssertion dgn-np:NP623254.RAvCgZjy9iWCYyiraQ3l9WAvVs1j8ho3LuebLuxOYP3fs130_assertion;
    np:hasProvenance dgn-np:NP623254.RAvCgZjy9iWCYyiraQ3l9WAvVs1j8ho3LuebLuxOYP3fs130_provenance;
    np:hasPublicationInfo dgn-np:NP623254.RAvCgZjy9iWCYyiraQ3l9WAvVs1j8ho3LuebLuxOYP3fs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP623254.RAvCgZjy9iWCYyiraQ3l9WAvVs1j8ho3LuebLuxOYP3fs130_assertion a np:Assertion .
  
  dgn-np:NP623254.RAvCgZjy9iWCYyiraQ3l9WAvVs1j8ho3LuebLuxOYP3fs130_provenance a np:Provenance .
  
  dgn-np:NP623254.RAvCgZjy9iWCYyiraQ3l9WAvVs1j8ho3LuebLuxOYP3fs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP623254.RAvCgZjy9iWCYyiraQ3l9WAvVs1j8ho3LuebLuxOYP3fs130_assertion {
  miriam-gene:641 a ncit:C16612 .
  
  lld:C0006142 a ncit:C7057 .
  
  dgn-gda:DGN341066ff3c1a3ef4a140ae3a51afb306 sio:SIO_000628 miriam-gene:641, lld:C0006142;
    a sio:SIO_001121 .
}

dgn-np:NP623254.RAvCgZjy9iWCYyiraQ3l9WAvVs1j8ho3LuebLuxOYP3fs130_provenance {
  dgn-np:NP623254.RAvCgZjy9iWCYyiraQ3l9WAvVs1j8ho3LuebLuxOYP3fs130_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-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:NP623254.RAvCgZjy9iWCYyiraQ3l9WAvVs1j8ho3LuebLuxOYP3fs130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:16+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" .
}