@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP568723.RAs_Y_uCX2b7c4vosVIR_BnFYRooDrxZIkHc3gKQWYnWY> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v3.0.0/void/> .

dgn-np:NP568723.RAs_Y_uCX2b7c4vosVIR_BnFYRooDrxZIkHc3gKQWYnWY130_head {
  this: np:hasAssertion dgn-np:NP568723.RAs_Y_uCX2b7c4vosVIR_BnFYRooDrxZIkHc3gKQWYnWY130_assertion;
    np:hasProvenance dgn-np:NP568723.RAs_Y_uCX2b7c4vosVIR_BnFYRooDrxZIkHc3gKQWYnWY130_provenance;
    np:hasPublicationInfo dgn-np:NP568723.RAs_Y_uCX2b7c4vosVIR_BnFYRooDrxZIkHc3gKQWYnWY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP568723.RAs_Y_uCX2b7c4vosVIR_BnFYRooDrxZIkHc3gKQWYnWY130_assertion a np:Assertion .
  
  dgn-np:NP568723.RAs_Y_uCX2b7c4vosVIR_BnFYRooDrxZIkHc3gKQWYnWY130_provenance a np:Provenance .
  
  dgn-np:NP568723.RAs_Y_uCX2b7c4vosVIR_BnFYRooDrxZIkHc3gKQWYnWY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP568723.RAs_Y_uCX2b7c4vosVIR_BnFYRooDrxZIkHc3gKQWYnWY130_assertion {
  miriam-gene:4360 a ncit:C16612 .
  
  lld:C0596263 a ncit:C7057 .
  
  dgn-gda:DGNbde943594a0eba44cd4d2ae8957229f3 sio:SIO_000628 miriam-gene:4360, lld:C0596263;
    a sio:SIO_001121 .
}

dgn-np:NP568723.RAs_Y_uCX2b7c4vosVIR_BnFYRooDrxZIkHc3gKQWYnWY130_provenance {
  dgn-np:NP568723.RAs_Y_uCX2b7c4vosVIR_BnFYRooDrxZIkHc3gKQWYnWY130_assertion dcterms:description
      "[Loss-of-heterozygosity (LOH) that retains the mutant MMR allele and epigenetic silencing of MMR genes are associated with an increased mutation rate that drives carcinogenesis as well as microsatellite instability that is a hallmark of LS/HNPCC.]. 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:23572416;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP568723.RAs_Y_uCX2b7c4vosVIR_BnFYRooDrxZIkHc3gKQWYnWY130_publicationInfo {
  this: dcterms:created "2015-08-25T14:43:18+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:disgenetv3.0rdf;
    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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}