@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP910682.RAnyOuyJ27KveXQBcN0mdc5CuP5A4xSuBTRKf7jCHl7vI> .
@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:NP910682.RAnyOuyJ27KveXQBcN0mdc5CuP5A4xSuBTRKf7jCHl7vI130_head {
  this: np:hasAssertion dgn-np:NP910682.RAnyOuyJ27KveXQBcN0mdc5CuP5A4xSuBTRKf7jCHl7vI130_assertion;
    np:hasProvenance dgn-np:NP910682.RAnyOuyJ27KveXQBcN0mdc5CuP5A4xSuBTRKf7jCHl7vI130_provenance;
    np:hasPublicationInfo dgn-np:NP910682.RAnyOuyJ27KveXQBcN0mdc5CuP5A4xSuBTRKf7jCHl7vI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP910682.RAnyOuyJ27KveXQBcN0mdc5CuP5A4xSuBTRKf7jCHl7vI130_assertion a np:Assertion .
  
  dgn-np:NP910682.RAnyOuyJ27KveXQBcN0mdc5CuP5A4xSuBTRKf7jCHl7vI130_provenance a np:Provenance .
  
  dgn-np:NP910682.RAnyOuyJ27KveXQBcN0mdc5CuP5A4xSuBTRKf7jCHl7vI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP910682.RAnyOuyJ27KveXQBcN0mdc5CuP5A4xSuBTRKf7jCHl7vI130_assertion {
  miriam-gene:4436 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGN84c73502b79550d2105b85873bd60aaf sio:SIO_000628 miriam-gene:4436, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP910682.RAnyOuyJ27KveXQBcN0mdc5CuP5A4xSuBTRKf7jCHl7vI130_provenance {
  dgn-np:NP910682.RAnyOuyJ27KveXQBcN0mdc5CuP5A4xSuBTRKf7jCHl7vI130_assertion dcterms:description
      "[The Lynch syndrome (LS) is an inherited cancer syndrome showing a preponderance of colorectal cancer (CRC) in context with endometrial cancer and several other extracolonic cancers, which is due to pathogenic mutations in the mismatch repair (MMR) genes, MLH1, MSH2, MSH6, and PMS2.]. 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:21769135;
    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:NP910682.RAnyOuyJ27KveXQBcN0mdc5CuP5A4xSuBTRKf7jCHl7vI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:36+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" .
}