@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc> .
@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:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_head {
  this: np:hasAssertion dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_assertion ;
    np:hasProvenance dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_provenance ;
    np:hasPublicationInfo dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_assertion a np:Assertion .
  dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_provenance a np:Provenance .
  dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  lld:C0006277 a ncit:C7057 .
  dgn-gda:DGN3587b0c9b892507f57f2825d9a94c047 sio:SIO_000628 miriam-gene:1080 , lld:C0006277 ;
    a sio:SIO_001121 .
}
dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_provenance {
  dgn-np:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_assertion dcterms:description "[It serves both to alert clinicians to consider CFTR-related disease in both young and elderly patients with persistent neutrophilic bronchitis, and to highlight the potential utility of future genetic testing for CFTR abnormalities in patients with asthma and recurrent bronchitis or pansinusitis, and the role of nebulized hypertonic saline as a therapeutic option in these 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:22332135 ;
    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:NP364469.RAUAvuSHyFq1u9Q0P1AluqlhfOZ9d2Tpm8On_wiDnQYLc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:33+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" .
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}