@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP280517.RAl7EM9XWIVS-KuH1dVsnmdRNK2sw-7O9sl05Ctxutkoc> .
@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:NP280517.RAl7EM9XWIVS-KuH1dVsnmdRNK2sw-7O9sl05Ctxutkoc130_head {
  this: np:hasAssertion dgn-np:NP280517.RAl7EM9XWIVS-KuH1dVsnmdRNK2sw-7O9sl05Ctxutkoc130_assertion;
    np:hasProvenance dgn-np:NP280517.RAl7EM9XWIVS-KuH1dVsnmdRNK2sw-7O9sl05Ctxutkoc130_provenance;
    np:hasPublicationInfo dgn-np:NP280517.RAl7EM9XWIVS-KuH1dVsnmdRNK2sw-7O9sl05Ctxutkoc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP280517.RAl7EM9XWIVS-KuH1dVsnmdRNK2sw-7O9sl05Ctxutkoc130_assertion a np:Assertion .
  
  dgn-np:NP280517.RAl7EM9XWIVS-KuH1dVsnmdRNK2sw-7O9sl05Ctxutkoc130_provenance a np:Provenance .
  
  dgn-np:NP280517.RAl7EM9XWIVS-KuH1dVsnmdRNK2sw-7O9sl05Ctxutkoc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP280517.RAl7EM9XWIVS-KuH1dVsnmdRNK2sw-7O9sl05Ctxutkoc130_assertion {
  miriam-gene:864 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN7c216d5f5889dfae01e6cfc92efe35f1 sio:SIO_000628 miriam-gene:864, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP280517.RAl7EM9XWIVS-KuH1dVsnmdRNK2sw-7O9sl05Ctxutkoc130_provenance {
  dgn-np:NP280517.RAl7EM9XWIVS-KuH1dVsnmdRNK2sw-7O9sl05Ctxutkoc130_assertion dcterms:description
      "[RUNX3 is frequently inactivated in human breast cancer cell lines and cancer samples by hemizygous deletion of the Runx3 gene, hypermethylation of the Runx3 promoter, or cytoplasmic sequestration of RUNX3 protein.]. 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:22275124;
    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:NP280517.RAl7EM9XWIVS-KuH1dVsnmdRNK2sw-7O9sl05Ctxutkoc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:38+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" .
}