@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP757953.RAus9YCWlsBfBKZ1Nq2eCY1diOOOG92f9zzvOPKaTLR7I> .
@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:NP757953.RAus9YCWlsBfBKZ1Nq2eCY1diOOOG92f9zzvOPKaTLR7I130_head {
  this: np:hasAssertion dgn-np:NP757953.RAus9YCWlsBfBKZ1Nq2eCY1diOOOG92f9zzvOPKaTLR7I130_assertion;
    np:hasProvenance dgn-np:NP757953.RAus9YCWlsBfBKZ1Nq2eCY1diOOOG92f9zzvOPKaTLR7I130_provenance;
    np:hasPublicationInfo dgn-np:NP757953.RAus9YCWlsBfBKZ1Nq2eCY1diOOOG92f9zzvOPKaTLR7I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP757953.RAus9YCWlsBfBKZ1Nq2eCY1diOOOG92f9zzvOPKaTLR7I130_assertion a np:Assertion .
  
  dgn-np:NP757953.RAus9YCWlsBfBKZ1Nq2eCY1diOOOG92f9zzvOPKaTLR7I130_provenance a np:Provenance .
  
  dgn-np:NP757953.RAus9YCWlsBfBKZ1Nq2eCY1diOOOG92f9zzvOPKaTLR7I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP757953.RAus9YCWlsBfBKZ1Nq2eCY1diOOOG92f9zzvOPKaTLR7I130_assertion {
  miriam-gene:4595 a ncit:C16612 .
  
  lld:C0009402 a ncit:C7057 .
  
  dgn-gda:DGN66a87524df1c820e5ca4378fe8b525b0 sio:SIO_000628 miriam-gene:4595, lld:C0009402;
    a sio:SIO_001121 .
}

dgn-np:NP757953.RAus9YCWlsBfBKZ1Nq2eCY1diOOOG92f9zzvOPKaTLR7I130_provenance {
  dgn-np:NP757953.RAus9YCWlsBfBKZ1Nq2eCY1diOOOG92f9zzvOPKaTLR7I130_assertion dcterms:description
      "[CRC patients carrying monoallelic MUTYH mutations harbor more frequently concomitant MSH6 mutations than patients without them, thus suggesting that both genes could act cooperatively and confer together an increased CRC risk.]. 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:19685280;
    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:NP757953.RAus9YCWlsBfBKZ1Nq2eCY1diOOOG92f9zzvOPKaTLR7I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:28+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" .
}