@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP583879.RAY9mdgY2LOb8iDC39vwjhzLNBQRWOWCCEpuAdLmJEcBg> .
@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:NP583879.RAY9mdgY2LOb8iDC39vwjhzLNBQRWOWCCEpuAdLmJEcBg130_head {
  this: np:hasAssertion dgn-np:NP583879.RAY9mdgY2LOb8iDC39vwjhzLNBQRWOWCCEpuAdLmJEcBg130_assertion;
    np:hasProvenance dgn-np:NP583879.RAY9mdgY2LOb8iDC39vwjhzLNBQRWOWCCEpuAdLmJEcBg130_provenance;
    np:hasPublicationInfo dgn-np:NP583879.RAY9mdgY2LOb8iDC39vwjhzLNBQRWOWCCEpuAdLmJEcBg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP583879.RAY9mdgY2LOb8iDC39vwjhzLNBQRWOWCCEpuAdLmJEcBg130_assertion a np:Assertion .
  
  dgn-np:NP583879.RAY9mdgY2LOb8iDC39vwjhzLNBQRWOWCCEpuAdLmJEcBg130_provenance a np:Provenance .
  
  dgn-np:NP583879.RAY9mdgY2LOb8iDC39vwjhzLNBQRWOWCCEpuAdLmJEcBg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP583879.RAY9mdgY2LOb8iDC39vwjhzLNBQRWOWCCEpuAdLmJEcBg130_assertion {
  miriam-gene:23671 a ncit:C16612 .
  
  lld:C0024623 a ncit:C7057 .
  
  dgn-gda:DGN2a9347a41e83093fbc6bcf0de158e9fe sio:SIO_000628 miriam-gene:23671, lld:C0024623;
    a sio:SIO_001121 .
}

dgn-np:NP583879.RAY9mdgY2LOb8iDC39vwjhzLNBQRWOWCCEpuAdLmJEcBg130_provenance {
  dgn-np:NP583879.RAY9mdgY2LOb8iDC39vwjhzLNBQRWOWCCEpuAdLmJEcBg130_assertion dcterms:description
      "[Hypermethylation of TPEF (a growth inhibitor), PTGER3 (a prostaglandin receptor isoform), and MINT31 (a promoter locus regulating calcium channels that is involved in p53 mutation) discriminated NIN and GC from normal mucosa, suggesting an early role as initiating events, whereas hypermethylation at ARGHAP20 developed with the progression from NIN to GC.]. 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:22179688;
    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:NP583879.RAY9mdgY2LOb8iDC39vwjhzLNBQRWOWCCEpuAdLmJEcBg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:51+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" .
}