@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc> .
@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:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_head {
  this: np:hasAssertion dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_assertion;
    np:hasProvenance dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_provenance;
    np:hasPublicationInfo dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_assertion a np:Assertion .
  
  dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_provenance a np:Provenance .
  
  dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_assertion {
  miriam-gene:4353 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGN63e0f897e5e9d30aa0223e42d605889e sio:SIO_000628 miriam-gene:4353, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_provenance {
  dgn-np:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_assertion dcterms:description
      "[Cystic fibrosis is a debilitating lung disease due to mutations in the cystic fibrosis transmembrane conductance regulator protein (CFTR) and is associated with chronic infections resulting in elevated myeloperoxidase activity and generation of hypochlorous acid (HOCl).]. 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:20799947;
    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:NP886956.RADLSW4vI2X9_SsytdR_DaOExQD0CJk0QIUA7P4MSYXuc130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:04+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" .
}