@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4> .
@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 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:NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_head {
   this: np:hasAssertion dgn-np:NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_assertion ;
    np:hasProvenance dgn-np:NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_provenance ;
    np:hasPublicationInfo dgn-np:NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_assertion a np:Assertion .
  dgn-np:NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_provenance a np:Provenance .
  dgn-np:NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_assertion {
   miriam-gene:1080 a ncit:C16612 .
  lld:C0024115 a ncit:C7057 .
  dgn-gda:DGN4dc007d976f6a1632716824e0a239fd2 sio:SIO_000628 miriam-gene:1080 , lld:C0024115 ;
    a sio:SIO_001122 .
}
dgn-np:NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_provenance {
   dgn-np:NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_assertion dct:description "[As it is known that certain CFTR variants have consequences on the function of CFTR protein, the aim of this study was to examine the possible role of F508del, M470V, Tn locus, and R75Q variants in COPD development and modulation.]. 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:18652532 ;
    prov:wasDerivedFrom dgn-void:gad-20130706 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:gad-20130706 pav:importedOn "2013-07-06"^^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:NP46880.RAoCVo639wO66MRMwL5ctS1YkZ94_wMUjbAPg62Rw8nG4130_publicationInfo {
   this: dct:created "2014-10-02T12:32:21+02:00"^^xsd:dateTime ;
    dct:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dct:rightsHolder dgn-void:IBIGroup ;
    dct:subject sio:SIO_000983 ;
    prv:usedData dgn-void:disgenetrdf ;
    pav:authoredBy orcid:0000-0001-5999-6269 , orcid:0000-0002-7534-7661 , orcid:0000-0002-9383-528X , orcid:0000-0003-0169-8159 , orcid:0000-0003-1244-7654 ;
    pav:createdBy orcid:0000-0003-0169-8159 ;
    pav:version "v2.1.0.0" .
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}