@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP853869.RAkujk0P8wy9av_jVZ_qUa6Qor_E88YoO1yBr4Iuj9vQA> .
@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:NP853869.RAkujk0P8wy9av_jVZ_qUa6Qor_E88YoO1yBr4Iuj9vQA130_head {
  this: np:hasAssertion dgn-np:NP853869.RAkujk0P8wy9av_jVZ_qUa6Qor_E88YoO1yBr4Iuj9vQA130_assertion;
    np:hasProvenance dgn-np:NP853869.RAkujk0P8wy9av_jVZ_qUa6Qor_E88YoO1yBr4Iuj9vQA130_provenance;
    np:hasPublicationInfo dgn-np:NP853869.RAkujk0P8wy9av_jVZ_qUa6Qor_E88YoO1yBr4Iuj9vQA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP853869.RAkujk0P8wy9av_jVZ_qUa6Qor_E88YoO1yBr4Iuj9vQA130_assertion a np:Assertion .
  
  dgn-np:NP853869.RAkujk0P8wy9av_jVZ_qUa6Qor_E88YoO1yBr4Iuj9vQA130_provenance a np:Provenance .
  
  dgn-np:NP853869.RAkujk0P8wy9av_jVZ_qUa6Qor_E88YoO1yBr4Iuj9vQA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP853869.RAkujk0P8wy9av_jVZ_qUa6Qor_E88YoO1yBr4Iuj9vQA130_assertion {
  miriam-gene:4292 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGNc1fb74ea99387c99b540901a5a57666b sio:SIO_000628 miriam-gene:4292, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP853869.RAkujk0P8wy9av_jVZ_qUa6Qor_E88YoO1yBr4Iuj9vQA130_provenance {
  dgn-np:NP853869.RAkujk0P8wy9av_jVZ_qUa6Qor_E88YoO1yBr4Iuj9vQA130_assertion dcterms:description
      "[The authors were able to replicate the association between the CRC susceptibility loci on chromosomes 8q23.3 and 11q23 and the risk of developing CRC in patients with Lynch syndrome, but the association could only be detected in MLH1 mutation carriers in this study.]. 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:21097774;
    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:NP853869.RAkujk0P8wy9av_jVZ_qUa6Qor_E88YoO1yBr4Iuj9vQA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:48:11+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" .
}