@prefix dct: <http://purl.org/dc/terms/> .
@prefix orcid: <http://orcid.org/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U> .
@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:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_head {
  this: np:hasAssertion dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_assertion ;
    np:hasProvenance dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_provenance ;
    np:hasPublicationInfo dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_assertion a np:Assertion .
  dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_provenance a np:Provenance .
  dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  lld:C0004096 a ncit:C7057 .
  dgn-gda:DGNadbd3185a779e38b7eeefab16f0282d1 sio:SIO_000628 miriam-gene:1080 , lld:C0004096 ;
    a sio:SIO_001122 .
}
dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_provenance {
  dgn-np:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_assertion dct:description "[In order to investigate the incidence of cystic fibrosis transmembrane conductance regulator (CFTR) gene mutations and unclassified variants in chronic pulmonary disease in children and adults, we studied 20 patients with asthma, 19 with disseminated bronchiectasis (DB) of unknown aetiology, and 12 patients with chronic obstructive pulmonary disease (COPD), and compared the results to 52 subjects from the general Greek population.]. 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:11354633 ;
    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:NP46876.RAjxKj70CX2bzO_tceOpxlQE3qhRLiiQCmUBm1bzi86-U130_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" .
}