@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E> .
@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/> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/> .
@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/resource/nanopub/> .
@prefix dgn-gda: <http://rdf.disgenet.org/resource/gda/> .
@prefix dgn-void: <http://rdf.disgenet.org/v4.0.0/void/> .

dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_head {
  this: np:hasAssertion dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_assertion;
    np:hasProvenance dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_provenance;
    np:hasPublicationInfo dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_assertion a np:Assertion .
  
  dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_provenance a np:Provenance .
  
  dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGNe5784daa7a8ec260c50ee4870e341af7 sio:SIO_000628 miriam-gene:1080, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_provenance {
  dgn-np:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_assertion dcterms:description
      "[Cystic Fibrosis (CF) is an autosomal recessive disorder due to mutations in the CF transmembrane conductance regulator (CFTR) gene that lead to defective ion transport in the conducting pulmonary airways and exocrine glands.]. 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:18600482;
    prov:wasDerivedFrom dgn-void:befree-2016;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP680281.RAE6UnbutNN0ADnRLfdPEoEEiuld-ekQSD2F37Xd6Nq0E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:53+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:disgenetv3.0rdf;
    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 "v4.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v4.0.0" .
}