@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP467686.RAmfrd0jNEls45GwJg_teRsLfdPjCgDUvtpEAcVug4Xq4> .
@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:NP467686.RAmfrd0jNEls45GwJg_teRsLfdPjCgDUvtpEAcVug4Xq4130_head {
  this: np:hasAssertion dgn-np:NP467686.RAmfrd0jNEls45GwJg_teRsLfdPjCgDUvtpEAcVug4Xq4130_assertion;
    np:hasProvenance dgn-np:NP467686.RAmfrd0jNEls45GwJg_teRsLfdPjCgDUvtpEAcVug4Xq4130_provenance;
    np:hasPublicationInfo dgn-np:NP467686.RAmfrd0jNEls45GwJg_teRsLfdPjCgDUvtpEAcVug4Xq4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP467686.RAmfrd0jNEls45GwJg_teRsLfdPjCgDUvtpEAcVug4Xq4130_assertion a np:Assertion .
  
  dgn-np:NP467686.RAmfrd0jNEls45GwJg_teRsLfdPjCgDUvtpEAcVug4Xq4130_provenance a np:Provenance .
  
  dgn-np:NP467686.RAmfrd0jNEls45GwJg_teRsLfdPjCgDUvtpEAcVug4Xq4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP467686.RAmfrd0jNEls45GwJg_teRsLfdPjCgDUvtpEAcVug4Xq4130_assertion {
  miriam-gene:2956 a ncit:C16612 .
  
  lld:C1333990 a ncit:C7057 .
  
  dgn-gda:DGNd5f116d9c88e76933337fce3aa4823eb sio:SIO_000628 miriam-gene:2956, lld:C1333990;
    a sio:SIO_001121 .
}

dgn-np:NP467686.RAmfrd0jNEls45GwJg_teRsLfdPjCgDUvtpEAcVug4Xq4130_provenance {
  dgn-np:NP467686.RAmfrd0jNEls45GwJg_teRsLfdPjCgDUvtpEAcVug4Xq4130_assertion dcterms:description
      "[Germline inactivation of MMR genes (hMLH1, hMSH2, hMSH6, and hPMS2) underlies the hereditary CRC with MMR defect (Lynch syndrome) and epigenetic silencing of hMLH1 gene causes the sporadic CRC with MMR defect.]. 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:15528793;
    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:NP467686.RAmfrd0jNEls45GwJg_teRsLfdPjCgDUvtpEAcVug4Xq4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:16+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" .
}