@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ> .
@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:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_head {
  this: np:hasAssertion dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_assertion;
    np:hasProvenance dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_provenance;
    np:hasPublicationInfo dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_assertion a np:Assertion .
  
  dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_provenance a np:Provenance .
  
  dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_assertion {
  miriam-gene:2272 a ncit:C16612 .
  
  lld:C0149925 a ncit:C7057 .
  
  dgn-gda:DGNf5a9c7432af5f514e7e3830a24728281 sio:SIO_000628 miriam-gene:2272, lld:C0149925;
    a sio:SIO_001121 .
}

dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_provenance {
  dgn-np:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_assertion dcterms:description
      "[To determine whether some individuals have increased fragility of FRA3B that might increase the risk for breakage or deletion in 3p14.2, fragile site expression was examined in smokers, nonsmokers, and small cell lung cancer (SCLC) patients.]. 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:12007194;
    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:NP263668.RADeI2UHjIbRfwb9Px0gpOnXMAPdJrVzDBvG7juvFZmsQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:27+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" .
}