@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP155493.RAcN1HxNb7pigQfxoi07iKqgjuLBBERJJIyzgoTP0uuGc> .
@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:NP155493.RAcN1HxNb7pigQfxoi07iKqgjuLBBERJJIyzgoTP0uuGc130_head {
  this: np:hasAssertion dgn-np:NP155493.RAcN1HxNb7pigQfxoi07iKqgjuLBBERJJIyzgoTP0uuGc130_assertion;
    np:hasProvenance dgn-np:NP155493.RAcN1HxNb7pigQfxoi07iKqgjuLBBERJJIyzgoTP0uuGc130_provenance;
    np:hasPublicationInfo dgn-np:NP155493.RAcN1HxNb7pigQfxoi07iKqgjuLBBERJJIyzgoTP0uuGc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP155493.RAcN1HxNb7pigQfxoi07iKqgjuLBBERJJIyzgoTP0uuGc130_assertion a np:Assertion .
  
  dgn-np:NP155493.RAcN1HxNb7pigQfxoi07iKqgjuLBBERJJIyzgoTP0uuGc130_provenance a np:Provenance .
  
  dgn-np:NP155493.RAcN1HxNb7pigQfxoi07iKqgjuLBBERJJIyzgoTP0uuGc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP155493.RAcN1HxNb7pigQfxoi07iKqgjuLBBERJJIyzgoTP0uuGc130_assertion {
  miriam-gene:9401 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGNacac1f3d5dbb081bbc868b1368cbcc36 sio:SIO_000628 miriam-gene:9401, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP155493.RAcN1HxNb7pigQfxoi07iKqgjuLBBERJJIyzgoTP0uuGc130_provenance {
  dgn-np:NP155493.RAcN1HxNb7pigQfxoi07iKqgjuLBBERJJIyzgoTP0uuGc130_assertion dcterms:description
      "[Mutations in three of the five known family members in humans, BLM, WRN and RECQL4, give rise to disorders that are characterized by predisposition to cancer and premature aging, emphasizing the importance of studying the RecQ proteins and their cellular activities.]. 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:17364146;
    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:NP155493.RAcN1HxNb7pigQfxoi07iKqgjuLBBERJJIyzgoTP0uuGc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}