@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP766498.RAB4QAn14ngCdPf5WThByEa0cGB8SlBYSFtdTw3OcRTIM> .
@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:NP766498.RAB4QAn14ngCdPf5WThByEa0cGB8SlBYSFtdTw3OcRTIM130_head {
  this: np:hasAssertion dgn-np:NP766498.RAB4QAn14ngCdPf5WThByEa0cGB8SlBYSFtdTw3OcRTIM130_assertion ;
    np:hasProvenance dgn-np:NP766498.RAB4QAn14ngCdPf5WThByEa0cGB8SlBYSFtdTw3OcRTIM130_provenance ;
    np:hasPublicationInfo dgn-np:NP766498.RAB4QAn14ngCdPf5WThByEa0cGB8SlBYSFtdTw3OcRTIM130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP766498.RAB4QAn14ngCdPf5WThByEa0cGB8SlBYSFtdTw3OcRTIM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP766498.RAB4QAn14ngCdPf5WThByEa0cGB8SlBYSFtdTw3OcRTIM130_assertion {
  miriam-gene:55511 a ncit:C16612 .
  lld:C0242379 a ncit:C7057 .
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    a sio:SIO_001121 .
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dgn-np:NP766498.RAB4QAn14ngCdPf5WThByEa0cGB8SlBYSFtdTw3OcRTIM130_provenance {
  dgn-np:NP766498.RAB4QAn14ngCdPf5WThByEa0cGB8SlBYSFtdTw3OcRTIM130_assertion dcterms:description "[We studied robust gene signature (RGS) in lung cancer by using an approach of integrating a highly diverse collection of cancer genome-wide datasets, which were six public microarray datasets, one pair of Suppression Subtractive Hybridization EST library, one pair of Serial Analysis of Gene Expression (SAGE) experiments, and 191 Loss of Heterozygosity (LOH) reports obtained from 388 publications.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
    wi:evidence dgn-void:source_evidence_literature ;
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    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 ;
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dgn-np:NP766498.RAB4QAn14ngCdPf5WThByEa0cGB8SlBYSFtdTw3OcRTIM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:44+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}