@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP834505.RAtvcQTuIttY_VBfjnRoWIrf4f2CD0nf6x5Y7a1nwXuVw> .
@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:NP834505.RAtvcQTuIttY_VBfjnRoWIrf4f2CD0nf6x5Y7a1nwXuVw130_head {
  this: np:hasAssertion dgn-np:NP834505.RAtvcQTuIttY_VBfjnRoWIrf4f2CD0nf6x5Y7a1nwXuVw130_assertion;
    np:hasProvenance dgn-np:NP834505.RAtvcQTuIttY_VBfjnRoWIrf4f2CD0nf6x5Y7a1nwXuVw130_provenance;
    np:hasPublicationInfo dgn-np:NP834505.RAtvcQTuIttY_VBfjnRoWIrf4f2CD0nf6x5Y7a1nwXuVw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP834505.RAtvcQTuIttY_VBfjnRoWIrf4f2CD0nf6x5Y7a1nwXuVw130_assertion a np:Assertion .
  
  dgn-np:NP834505.RAtvcQTuIttY_VBfjnRoWIrf4f2CD0nf6x5Y7a1nwXuVw130_provenance a np:Provenance .
  
  dgn-np:NP834505.RAtvcQTuIttY_VBfjnRoWIrf4f2CD0nf6x5Y7a1nwXuVw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP834505.RAtvcQTuIttY_VBfjnRoWIrf4f2CD0nf6x5Y7a1nwXuVw130_assertion {
  miriam-gene:104 a ncit:C16612 .
  
  lld:C0242379 a ncit:C7057 .
  
  dgn-gda:DGNe28630bf2c4a61a7d7f99d72c8cf47e5 sio:SIO_000628 miriam-gene:104, lld:C0242379;
    a sio:SIO_001121 .
}

dgn-np:NP834505.RAtvcQTuIttY_VBfjnRoWIrf4f2CD0nf6x5Y7a1nwXuVw130_provenance {
  dgn-np:NP834505.RAtvcQTuIttY_VBfjnRoWIrf4f2CD0nf6x5Y7a1nwXuVw130_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:NP834505.RAtvcQTuIttY_VBfjnRoWIrf4f2CD0nf6x5Y7a1nwXuVw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:30+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" .
}