@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E> .
@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:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_head {
  this: np:hasAssertion dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_assertion;
    np:hasProvenance dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_provenance;
    np:hasPublicationInfo dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_assertion a np:Assertion .
  
  dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_provenance a np:Provenance .
  
  dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGNd71c8c12f9f7ee897dcc2efe46362b31 sio:SIO_000628 miriam-gene:1080, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_provenance {
  dgn-np:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_assertion dcterms:description
      "[Mutations of CFTR gene are responsible for cystic fibrosis (CF) and other clinical conditions such as congenital absence of the vas deferens (CAVD), chronic pancreatitis (IP), and idiopathic disseminated bronchiectasis (DBE) classified as CFTR-related disorders.]. 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:16379540;
    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:NP528494.RAyFhyNfmFMqLJPpzsUQq4UU09mXZnX_KTozY1zp3454E130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:44+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" .
}