@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o> .
@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:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_head {
  this: np:hasAssertion dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_assertion;
    np:hasProvenance dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_provenance;
    np:hasPublicationInfo dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_assertion a np:Assertion .
  
  dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_provenance a np:Provenance .
  
  dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_assertion {
  miriam-gene:1663 a ncit:C16612 .
  
  lld:C0278883 a ncit:C7057 .
  
  dgn-gda:DGNd7b906df182c48263779d9f88f1ecc4d sio:SIO_000628 miriam-gene:1663, lld:C0278883;
    a sio:SIO_001121 .
}

dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_provenance {
  dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_assertion dcterms:description
      "[In this report, we show that the helicase DDX11 is expressed at high levels in primary and metastatic melanoma, and that interfering with its expression leads to severe chromosome segregation defects, telomere shortening, and massive melanoma cell apoptosis.]. 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:23116066;
    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:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:59+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" .
}