@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP929439.RAfuCeQnDThW1YM76Lnj7bWF2aN3Dv33aV1k5lV3mo91Y> .
@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:NP929439.RAfuCeQnDThW1YM76Lnj7bWF2aN3Dv33aV1k5lV3mo91Y130_head {
  this: np:hasAssertion dgn-np:NP929439.RAfuCeQnDThW1YM76Lnj7bWF2aN3Dv33aV1k5lV3mo91Y130_assertion;
    np:hasProvenance dgn-np:NP929439.RAfuCeQnDThW1YM76Lnj7bWF2aN3Dv33aV1k5lV3mo91Y130_provenance;
    np:hasPublicationInfo dgn-np:NP929439.RAfuCeQnDThW1YM76Lnj7bWF2aN3Dv33aV1k5lV3mo91Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP929439.RAfuCeQnDThW1YM76Lnj7bWF2aN3Dv33aV1k5lV3mo91Y130_assertion a np:Assertion .
  
  dgn-np:NP929439.RAfuCeQnDThW1YM76Lnj7bWF2aN3Dv33aV1k5lV3mo91Y130_provenance a np:Provenance .
  
  dgn-np:NP929439.RAfuCeQnDThW1YM76Lnj7bWF2aN3Dv33aV1k5lV3mo91Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP929439.RAfuCeQnDThW1YM76Lnj7bWF2aN3Dv33aV1k5lV3mo91Y130_assertion {
  miriam-gene:7055 a ncit:C16612 .
  
  lld:C0008626 a ncit:C7057 .
  
  dgn-gda:DGN24d2912ab2bd3b2473337db3954b9f4f sio:SIO_000628 miriam-gene:7055, lld:C0008626;
    a sio:SIO_001121 .
}

dgn-np:NP929439.RAfuCeQnDThW1YM76Lnj7bWF2aN3Dv33aV1k5lV3mo91Y130_provenance {
  dgn-np:NP929439.RAfuCeQnDThW1YM76Lnj7bWF2aN3Dv33aV1k5lV3mo91Y130_assertion dcterms:description
      "[Peripheral blood lymphocyte cultures from 20 untreated UC patients and 24 controls were used to study chromosome instability by assessing telomeric associations (TAS), chromosome aberrations (CA), and sister chromatid exchanges (SCE).]. 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:11007232;
    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:NP929439.RAfuCeQnDThW1YM76Lnj7bWF2aN3Dv33aV1k5lV3mo91Y130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:30+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" .
}