@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q> .
@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/v4.0.0/void/> .
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_head {
  this: np:hasAssertion dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_assertion ;
    np:hasProvenance dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_provenance ;
    np:hasPublicationInfo dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_assertion a np:Assertion .
  dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_provenance a np:Provenance .
  dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  lld:C0009402 a ncit:C7057 .
  dgn-gda:DGNd1f8aa5cf9615913fc4b36a3116bce19 sio:SIO_000628 miriam-gene:4436 , lld:C0009402 ;
    a sio:SIO_001121 .
}
dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_provenance {
  dgn-np:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_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 eco:ECO_0000203 .
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP261630.RAuoqzsNO_m3UQkHIc9-j6_YggNGyVZslScoKR9K6uQ2Q130_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" .
}