@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP596969.RAadP-zqY_UuKpeU2TEYLljmKcWM_O4nREySEbVOWPlp0> .
@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:NP596969.RAadP-zqY_UuKpeU2TEYLljmKcWM_O4nREySEbVOWPlp0130_head {
  this: np:hasAssertion dgn-np:NP596969.RAadP-zqY_UuKpeU2TEYLljmKcWM_O4nREySEbVOWPlp0130_assertion ;
    np:hasProvenance dgn-np:NP596969.RAadP-zqY_UuKpeU2TEYLljmKcWM_O4nREySEbVOWPlp0130_provenance ;
    np:hasPublicationInfo dgn-np:NP596969.RAadP-zqY_UuKpeU2TEYLljmKcWM_O4nREySEbVOWPlp0130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP596969.RAadP-zqY_UuKpeU2TEYLljmKcWM_O4nREySEbVOWPlp0130_provenance a np:Provenance .
  dgn-np:NP596969.RAadP-zqY_UuKpeU2TEYLljmKcWM_O4nREySEbVOWPlp0130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP596969.RAadP-zqY_UuKpeU2TEYLljmKcWM_O4nREySEbVOWPlp0130_assertion {
  miriam-gene:729238 a ncit:C16612 .
  lld:C0242379 a ncit:C7057 .
  dgn-gda:DGN5e655c4ff1fce24967f8fc037f29244d sio:SIO_000628 miriam-gene:729238 , lld:C0242379 ;
    a sio:SIO_001121 .
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dgn-np:NP596969.RAadP-zqY_UuKpeU2TEYLljmKcWM_O4nREySEbVOWPlp0130_provenance {
  dgn-np:NP596969.RAadP-zqY_UuKpeU2TEYLljmKcWM_O4nREySEbVOWPlp0130_assertion dcterms:description "[To evaluate whether the accuracy of diagnosing lung cancer by evaluating sputa for cytologic atypia and genetic abnormalities is greater than that of conventional cytology alone, automated scoring of genetic abnormalities for 3p22.1 and 10q22.3 (SP-A) by fluorescence in situ hybridization (FISH) and conventional cytology was done on sputa from 35 subjects with lung cancer, 25 high-risk smokers, and 6 healthy control subjects.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en ;
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dgn-np:NP596969.RAadP-zqY_UuKpeU2TEYLljmKcWM_O4nREySEbVOWPlp0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:59+02:00"^^xsd:dateTime ;
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    dcterms:rightsHolder dgn-void:IBIGroup ;
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