@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP567031.RAq4PqrZEswWiBJcC4v8BdW2iM0vNhT3G5A7z9aDFaUZs> .
@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:NP567031.RAq4PqrZEswWiBJcC4v8BdW2iM0vNhT3G5A7z9aDFaUZs130_head {
   this: np:hasAssertion dgn-np:NP567031.RAq4PqrZEswWiBJcC4v8BdW2iM0vNhT3G5A7z9aDFaUZs130_assertion ;
    np:hasProvenance dgn-np:NP567031.RAq4PqrZEswWiBJcC4v8BdW2iM0vNhT3G5A7z9aDFaUZs130_provenance ;
    np:hasPublicationInfo dgn-np:NP567031.RAq4PqrZEswWiBJcC4v8BdW2iM0vNhT3G5A7z9aDFaUZs130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP567031.RAq4PqrZEswWiBJcC4v8BdW2iM0vNhT3G5A7z9aDFaUZs130_assertion a np:Assertion .
  dgn-np:NP567031.RAq4PqrZEswWiBJcC4v8BdW2iM0vNhT3G5A7z9aDFaUZs130_provenance a np:Provenance .
  dgn-np:NP567031.RAq4PqrZEswWiBJcC4v8BdW2iM0vNhT3G5A7z9aDFaUZs130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP567031.RAq4PqrZEswWiBJcC4v8BdW2iM0vNhT3G5A7z9aDFaUZs130_assertion {
   miriam-gene:79813 a ncit:C16612 .
  lld:C1527249 a ncit:C7057 .
  dgn-gda:DGN073b464567007291a42bf23d8e76e286 sio:SIO_000628 miriam-gene:79813 , lld:C1527249 ;
    a sio:SIO_001121 .
}
dgn-np:NP567031.RAq4PqrZEswWiBJcC4v8BdW2iM0vNhT3G5A7z9aDFaUZs130_provenance {
   dgn-np:NP567031.RAq4PqrZEswWiBJcC4v8BdW2iM0vNhT3G5A7z9aDFaUZs130_assertion dcterms:description "[We studied associations of genetic variants of folate metabolizing enzymes (MTHFR, MTR, and MTRR), DNA methyltransferase DNMT3b, and histone methyltransferases (EHMT1, EHMT2, and PRDM2), with colorectal cancers, with or without the CpG island methylator phenotype (CIMP), MLH1 hypermethylation, or microsatellite instability.]. 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:19843671 ;
    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:NP567031.RAq4PqrZEswWiBJcC4v8BdW2iM0vNhT3G5A7z9aDFaUZs130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:42+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" .
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}