@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP247418.RA21J9F29R8eilvVTapPmosupU497dtqFeuXDhVQSry74> .
@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:NP247418.RA21J9F29R8eilvVTapPmosupU497dtqFeuXDhVQSry74130_head {
  this: np:hasAssertion dgn-np:NP247418.RA21J9F29R8eilvVTapPmosupU497dtqFeuXDhVQSry74130_assertion;
    np:hasProvenance dgn-np:NP247418.RA21J9F29R8eilvVTapPmosupU497dtqFeuXDhVQSry74130_provenance;
    np:hasPublicationInfo dgn-np:NP247418.RA21J9F29R8eilvVTapPmosupU497dtqFeuXDhVQSry74130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP247418.RA21J9F29R8eilvVTapPmosupU497dtqFeuXDhVQSry74130_assertion a np:Assertion .
  
  dgn-np:NP247418.RA21J9F29R8eilvVTapPmosupU497dtqFeuXDhVQSry74130_provenance a np:Provenance .
  
  dgn-np:NP247418.RA21J9F29R8eilvVTapPmosupU497dtqFeuXDhVQSry74130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP247418.RA21J9F29R8eilvVTapPmosupU497dtqFeuXDhVQSry74130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  
  lld:C0476089 a ncit:C7057 .
  
  dgn-gda:DGN3f24b7353e1309e64eb833e0904604e6 sio:SIO_000628 miriam-gene:4436, lld:C0476089;
    a sio:SIO_001121 .
}

dgn-np:NP247418.RA21J9F29R8eilvVTapPmosupU497dtqFeuXDhVQSry74130_provenance {
  dgn-np:NP247418.RA21J9F29R8eilvVTapPmosupU497dtqFeuXDhVQSry74130_assertion dcterms:description
      "[These observations suggest that epigenetic changes in the MLH1 locus account for MSI in most cases of sporadic endometrial cancers and provide additional evidence that the MSH2 gene may contribute substantially to inherited forms of endometrial cancer.]. 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:10072435;
    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:NP247418.RA21J9F29R8eilvVTapPmosupU497dtqFeuXDhVQSry74130_publicationInfo {
  this: dcterms:created "2016-05-13T12:43:38+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" .
}