@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP164106.RAGZDw4tmYH9QEOGZExn_osd75E3Lt8LVImqrHLXJxPpg> .
@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:NP164106.RAGZDw4tmYH9QEOGZExn_osd75E3Lt8LVImqrHLXJxPpg130_head {
  this: np:hasAssertion dgn-np:NP164106.RAGZDw4tmYH9QEOGZExn_osd75E3Lt8LVImqrHLXJxPpg130_assertion;
    np:hasProvenance dgn-np:NP164106.RAGZDw4tmYH9QEOGZExn_osd75E3Lt8LVImqrHLXJxPpg130_provenance;
    np:hasPublicationInfo dgn-np:NP164106.RAGZDw4tmYH9QEOGZExn_osd75E3Lt8LVImqrHLXJxPpg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP164106.RAGZDw4tmYH9QEOGZExn_osd75E3Lt8LVImqrHLXJxPpg130_assertion a np:Assertion .
  
  dgn-np:NP164106.RAGZDw4tmYH9QEOGZExn_osd75E3Lt8LVImqrHLXJxPpg130_provenance a np:Provenance .
  
  dgn-np:NP164106.RAGZDw4tmYH9QEOGZExn_osd75E3Lt8LVImqrHLXJxPpg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP164106.RAGZDw4tmYH9QEOGZExn_osd75E3Lt8LVImqrHLXJxPpg130_assertion {
  miriam-gene:898 a ncit:C16612 .
  
  lld:C0006826 a ncit:C7057 .
  
  dgn-gda:DGN8cc9bc92c4fc43030f4bb21cd180a8f2 sio:SIO_000628 miriam-gene:898, lld:C0006826;
    a sio:SIO_001121 .
}

dgn-np:NP164106.RAGZDw4tmYH9QEOGZExn_osd75E3Lt8LVImqrHLXJxPpg130_provenance {
  dgn-np:NP164106.RAGZDw4tmYH9QEOGZExn_osd75E3Lt8LVImqrHLXJxPpg130_assertion dcterms:description
      "[When compared with previously reported results, SAIC successfully identifies most SCAs known to be of biological significance and associated with oncogenes (e.g., KRAS, CCNE1, and MYC) or tumor suppressor genes (e.g., CDKN2A/B).]. 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:22839576;
    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:NP164106.RAGZDw4tmYH9QEOGZExn_osd75E3Lt8LVImqrHLXJxPpg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}