@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8> .
@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:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_head {
  this: np:hasAssertion dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_assertion;
    np:hasProvenance dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_provenance;
    np:hasPublicationInfo dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_assertion a np:Assertion .
  
  dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_provenance a np:Provenance .
  
  dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_assertion {
  miriam-gene:5290 a ncit:C16612 .
  
  lld:C0024623 a ncit:C7057 .
  
  dgn-gda:DGN51bcfd0ba6c8894ce9355958a2d65ef1 sio:SIO_000628 miriam-gene:5290, lld:C0024623;
    a sio:SIO_001121 .
}

dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_provenance {
  dgn-np:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_assertion dcterms:description
      "[Integration of information on the genetic and epigenetic alterations revealed that the GCs with the CpG island methylator phenotype (CIMP) tended to have mutations of oncogenes, CTNNB1, ERBB2, KRAS, and PIK3CA.]. 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:23196062;
    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:NP334931.RAn5iqrTy8EhB1hc9dP1ubPhfner5H3pqSb8FXTFz0pj8130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:17+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" .
}