@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP692785.RAadFPvP_GXnnpUbSc7VBw7MHIeHoY5sghLyXK6K8IG74> .
@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:NP692785.RAadFPvP_GXnnpUbSc7VBw7MHIeHoY5sghLyXK6K8IG74130_head {
  this: np:hasAssertion dgn-np:NP692785.RAadFPvP_GXnnpUbSc7VBw7MHIeHoY5sghLyXK6K8IG74130_assertion;
    np:hasProvenance dgn-np:NP692785.RAadFPvP_GXnnpUbSc7VBw7MHIeHoY5sghLyXK6K8IG74130_provenance;
    np:hasPublicationInfo dgn-np:NP692785.RAadFPvP_GXnnpUbSc7VBw7MHIeHoY5sghLyXK6K8IG74130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP692785.RAadFPvP_GXnnpUbSc7VBw7MHIeHoY5sghLyXK6K8IG74130_assertion a np:Assertion .
  
  dgn-np:NP692785.RAadFPvP_GXnnpUbSc7VBw7MHIeHoY5sghLyXK6K8IG74130_provenance a np:Provenance .
  
  dgn-np:NP692785.RAadFPvP_GXnnpUbSc7VBw7MHIeHoY5sghLyXK6K8IG74130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP692785.RAadFPvP_GXnnpUbSc7VBw7MHIeHoY5sghLyXK6K8IG74130_assertion {
  miriam-gene:104 a ncit:C16612 .
  
  lld:C0684249 a ncit:C7057 .
  
  dgn-gda:DGN645012800e7abb07ed969ec940105d0d sio:SIO_000628 miriam-gene:104, lld:C0684249;
    a sio:SIO_001121 .
}

dgn-np:NP692785.RAadFPvP_GXnnpUbSc7VBw7MHIeHoY5sghLyXK6K8IG74130_provenance {
  dgn-np:NP692785.RAadFPvP_GXnnpUbSc7VBw7MHIeHoY5sghLyXK6K8IG74130_assertion dcterms:description
      "[Moreover, we found a high incidence of loss of heterozygosity at chromosome 21q22.3, where the ADAR2 locus is located, in NSCLC cell lines and primary tissues, suggesting that the downregulation of ADAR2 in lung cancer is associated with specific genetic losses.]. 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:22876301;
    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:NP692785.RAadFPvP_GXnnpUbSc7VBw7MHIeHoY5sghLyXK6K8IG74130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:01+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" .
}