@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP261565.RAW94gkX96oQA_BgU9NbOEE36NaKp_AnFcFKQklXE2OI4> .
@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:NP261565.RAW94gkX96oQA_BgU9NbOEE36NaKp_AnFcFKQklXE2OI4130_head {
  this: np:hasAssertion dgn-np:NP261565.RAW94gkX96oQA_BgU9NbOEE36NaKp_AnFcFKQklXE2OI4130_assertion;
    np:hasProvenance dgn-np:NP261565.RAW94gkX96oQA_BgU9NbOEE36NaKp_AnFcFKQklXE2OI4130_provenance;
    np:hasPublicationInfo dgn-np:NP261565.RAW94gkX96oQA_BgU9NbOEE36NaKp_AnFcFKQklXE2OI4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP261565.RAW94gkX96oQA_BgU9NbOEE36NaKp_AnFcFKQklXE2OI4130_assertion a np:Assertion .
  
  dgn-np:NP261565.RAW94gkX96oQA_BgU9NbOEE36NaKp_AnFcFKQklXE2OI4130_provenance a np:Provenance .
  
  dgn-np:NP261565.RAW94gkX96oQA_BgU9NbOEE36NaKp_AnFcFKQklXE2OI4130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP261565.RAW94gkX96oQA_BgU9NbOEE36NaKp_AnFcFKQklXE2OI4130_assertion {
  miriam-gene:864 a ncit:C16612 .
  
  lld:C0007137 a ncit:C7057 .
  
  dgn-gda:DGN2dcc4625b4473f7ade846c69f3d0f1f5 sio:SIO_000628 miriam-gene:864, lld:C0007137;
    a sio:SIO_001121 .
}

dgn-np:NP261565.RAW94gkX96oQA_BgU9NbOEE36NaKp_AnFcFKQklXE2OI4130_provenance {
  dgn-np:NP261565.RAW94gkX96oQA_BgU9NbOEE36NaKp_AnFcFKQklXE2OI4130_assertion dcterms:description
      "[The western blotting experiments showed that RUNX3 was not expressed in normal skin tissues, but it was overexpressed in all MM and SCC samples, and in five of the six BCC samples.]. 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:21623876;
    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:NP261565.RAW94gkX96oQA_BgU9NbOEE36NaKp_AnFcFKQklXE2OI4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:26+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" .
}