@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP359326.RAmGtarOzhVuo6cK4iqAgVnGG8tr66ornAuUhSR6aO5sA> .
@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:NP359326.RAmGtarOzhVuo6cK4iqAgVnGG8tr66ornAuUhSR6aO5sA130_head {
  this: np:hasAssertion dgn-np:NP359326.RAmGtarOzhVuo6cK4iqAgVnGG8tr66ornAuUhSR6aO5sA130_assertion;
    np:hasProvenance dgn-np:NP359326.RAmGtarOzhVuo6cK4iqAgVnGG8tr66ornAuUhSR6aO5sA130_provenance;
    np:hasPublicationInfo dgn-np:NP359326.RAmGtarOzhVuo6cK4iqAgVnGG8tr66ornAuUhSR6aO5sA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP359326.RAmGtarOzhVuo6cK4iqAgVnGG8tr66ornAuUhSR6aO5sA130_assertion a np:Assertion .
  
  dgn-np:NP359326.RAmGtarOzhVuo6cK4iqAgVnGG8tr66ornAuUhSR6aO5sA130_provenance a np:Provenance .
  
  dgn-np:NP359326.RAmGtarOzhVuo6cK4iqAgVnGG8tr66ornAuUhSR6aO5sA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP359326.RAmGtarOzhVuo6cK4iqAgVnGG8tr66ornAuUhSR6aO5sA130_assertion {
  miriam-gene:1612 a ncit:C16612 .
  
  lld:C1527249 a ncit:C7057 .
  
  dgn-gda:DGN3d2f5ddb99d6ae0b5b746fe807258537 sio:SIO_000628 miriam-gene:1612, lld:C1527249;
    a sio:SIO_001121 .
}

dgn-np:NP359326.RAmGtarOzhVuo6cK4iqAgVnGG8tr66ornAuUhSR6aO5sA130_provenance {
  dgn-np:NP359326.RAmGtarOzhVuo6cK4iqAgVnGG8tr66ornAuUhSR6aO5sA130_assertion dcterms:description
      "[The aim of this study was to investigate the methylation of the SFRP2, P16, DAPK1, HIC1, and MGMT genes, as well as the mutation of amino acid codons 12 and 13 of the KRAS gene in normal and tumor tissue DNA of patients diagnosed with sporadic colorectal cancer (SCRC).]. 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:20682398;
    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:NP359326.RAmGtarOzhVuo6cK4iqAgVnGG8tr66ornAuUhSR6aO5sA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:30+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" .
}