@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_head {
  this: np:hasAssertion dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_assertion;
    np:hasProvenance dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_provenance;
    np:hasPublicationInfo dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_assertion a np:Assertion .
  
  dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_provenance a np:Provenance .
  
  dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_assertion {
  miriam-gene:4595 a ncit:C16612 .
  
  lld:C0007097 a ncit:C7057 .
  
  dgn-gda:DGNab3c66aa5fdc42ff7f9e8f209b506867 sio:SIO_000628 miriam-gene:4595, lld:C0007097;
    a sio:SIO_001121 .
}

dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_provenance {
  dgn-np:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_assertion dcterms:description
      "[Biallelic germline mutations of MUTYH have been shown to predict familial and sporadic multiple colorectal adenomas and carcinomas, however, whether there is an association between single nucleotide polymorphisms (SNPs) of MUTYH and sporadic colorectal cancer (CRC) risk has remained unclear.]. 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:18271935;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP457838.RABNaAj7j1FP-f-rt4oq5NDd4hnsblDgG0imSC9tV4zJ4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:33+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}