@prefix bfo: <http://purl.obolibrary.org/obo/> .
@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP261627.RAN-ezgzUML5D1fM_RmA6gHIihHXnqhSFxKUAGH9QZ72E> .
@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 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/v4.0.0/void/> .

dgn-np:NP261627.RAN-ezgzUML5D1fM_RmA6gHIihHXnqhSFxKUAGH9QZ72E130_head {
  this: np:hasAssertion dgn-np:NP261627.RAN-ezgzUML5D1fM_RmA6gHIihHXnqhSFxKUAGH9QZ72E130_assertion;
    np:hasProvenance dgn-np:NP261627.RAN-ezgzUML5D1fM_RmA6gHIihHXnqhSFxKUAGH9QZ72E130_provenance;
    np:hasPublicationInfo dgn-np:NP261627.RAN-ezgzUML5D1fM_RmA6gHIihHXnqhSFxKUAGH9QZ72E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP261627.RAN-ezgzUML5D1fM_RmA6gHIihHXnqhSFxKUAGH9QZ72E130_assertion a np:Assertion .
  
  dgn-np:NP261627.RAN-ezgzUML5D1fM_RmA6gHIihHXnqhSFxKUAGH9QZ72E130_provenance a np:Provenance .
  
  dgn-np:NP261627.RAN-ezgzUML5D1fM_RmA6gHIihHXnqhSFxKUAGH9QZ72E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP261627.RAN-ezgzUML5D1fM_RmA6gHIihHXnqhSFxKUAGH9QZ72E130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNdafe10ebd894d033e95e123e73cac59b sio:SIO_000628 miriam-gene:4436, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP261627.RAN-ezgzUML5D1fM_RmA6gHIihHXnqhSFxKUAGH9QZ72E130_provenance {
  dgn-np:NP261627.RAN-ezgzUML5D1fM_RmA6gHIihHXnqhSFxKUAGH9QZ72E130_assertion dcterms:description
      "[Because the frequency of mutations in the mismatch repair genes (hMLH1 and hMSH2) is low in these tumors, we have investigated the role of mutational inactivation, methylation of the promoter region, and loss of heterozygosity (LOH) as a possible explanation for the mutator phenotype of RER+ colorectal cancer cell lines.]. 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:10468602;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy bfo:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date .
  
  dgn-void:source_evidence_literature a bfo:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP261627.RAN-ezgzUML5D1fM_RmA6gHIihHXnqhSFxKUAGH9QZ72E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:44+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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}