@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP213728.RAWW7lZqIGrS4QmiEzv6m9DPZ_wRT9qeiT5qCfaoWwrcU> .
@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:NP213728.RAWW7lZqIGrS4QmiEzv6m9DPZ_wRT9qeiT5qCfaoWwrcU130_head {
  this: np:hasAssertion dgn-np:NP213728.RAWW7lZqIGrS4QmiEzv6m9DPZ_wRT9qeiT5qCfaoWwrcU130_assertion;
    np:hasProvenance dgn-np:NP213728.RAWW7lZqIGrS4QmiEzv6m9DPZ_wRT9qeiT5qCfaoWwrcU130_provenance;
    np:hasPublicationInfo dgn-np:NP213728.RAWW7lZqIGrS4QmiEzv6m9DPZ_wRT9qeiT5qCfaoWwrcU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP213728.RAWW7lZqIGrS4QmiEzv6m9DPZ_wRT9qeiT5qCfaoWwrcU130_assertion a np:Assertion .
  
  dgn-np:NP213728.RAWW7lZqIGrS4QmiEzv6m9DPZ_wRT9qeiT5qCfaoWwrcU130_provenance a np:Provenance .
  
  dgn-np:NP213728.RAWW7lZqIGrS4QmiEzv6m9DPZ_wRT9qeiT5qCfaoWwrcU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP213728.RAWW7lZqIGrS4QmiEzv6m9DPZ_wRT9qeiT5qCfaoWwrcU130_assertion {
  miriam-gene:7799 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN9194974bd0f3d28bd1fc36c281373bde sio:SIO_000628 miriam-gene:7799, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP213728.RAWW7lZqIGrS4QmiEzv6m9DPZ_wRT9qeiT5qCfaoWwrcU130_provenance {
  dgn-np:NP213728.RAWW7lZqIGrS4QmiEzv6m9DPZ_wRT9qeiT5qCfaoWwrcU130_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:NP213728.RAWW7lZqIGrS4QmiEzv6m9DPZ_wRT9qeiT5qCfaoWwrcU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:58+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" .
}