@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP910698.RAqKZwrcHBIpqlr9xSqycje8ltGwDdx6bI_ahnYxNe3Cg> .
@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:NP910698.RAqKZwrcHBIpqlr9xSqycje8ltGwDdx6bI_ahnYxNe3Cg130_head {
  this: np:hasAssertion dgn-np:NP910698.RAqKZwrcHBIpqlr9xSqycje8ltGwDdx6bI_ahnYxNe3Cg130_assertion;
    np:hasProvenance dgn-np:NP910698.RAqKZwrcHBIpqlr9xSqycje8ltGwDdx6bI_ahnYxNe3Cg130_provenance;
    np:hasPublicationInfo dgn-np:NP910698.RAqKZwrcHBIpqlr9xSqycje8ltGwDdx6bI_ahnYxNe3Cg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP910698.RAqKZwrcHBIpqlr9xSqycje8ltGwDdx6bI_ahnYxNe3Cg130_assertion a np:Assertion .
  
  dgn-np:NP910698.RAqKZwrcHBIpqlr9xSqycje8ltGwDdx6bI_ahnYxNe3Cg130_provenance a np:Provenance .
  
  dgn-np:NP910698.RAqKZwrcHBIpqlr9xSqycje8ltGwDdx6bI_ahnYxNe3Cg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP910698.RAqKZwrcHBIpqlr9xSqycje8ltGwDdx6bI_ahnYxNe3Cg130_assertion {
  miriam-gene:5395 a ncit:C16612 .
  
  lld:C0007103 a ncit:C7057 .
  
  dgn-gda:DGN469db7a7797d9f20fefc4d2f80b0e30b sio:SIO_000628 miriam-gene:5395, lld:C0007103;
    a sio:SIO_001121 .
}

dgn-np:NP910698.RAqKZwrcHBIpqlr9xSqycje8ltGwDdx6bI_ahnYxNe3Cg130_provenance {
  dgn-np:NP910698.RAqKZwrcHBIpqlr9xSqycje8ltGwDdx6bI_ahnYxNe3Cg130_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:NP910698.RAqKZwrcHBIpqlr9xSqycje8ltGwDdx6bI_ahnYxNe3Cg130_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" .
}