@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE> .
@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:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_head {
  this: np:hasAssertion dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_assertion;
    np:hasProvenance dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_provenance;
    np:hasPublicationInfo dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_assertion a np:Assertion .
  
  dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_provenance a np:Provenance .
  
  dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_assertion {
  miriam-gene:3342 a ncit:C16612 .
  
  lld:C0007131 a ncit:C7057 .
  
  dgn-gda:DGN2fc2372b0c8d04380c4efb9bfaff6c0d sio:SIO_000628 miriam-gene:3342, lld:C0007131;
    a sio:SIO_001121 .
}

dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_provenance {
  dgn-np:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_assertion dcterms:description
      "[To identify early-stage genetic events that drive progression of NSCLC, we conducted a high-resolution array comparative genomic hybridization (CGH) study, using an array of 4,046 bacterial artificial chromosome clones to screen for DNA copy number changes associated with individual genes in 36 tumors obtained from patients in early stages of NSCLC.]. 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:18328944;
    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:NP905965.RAPdmv_TSrJw2oG5FSR91x4XdfAYJuoA5rX8LlCPcKYZE130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:16+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" .
}