@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1267561.RAUTSZRS87XHPY4xtstMfCxaiBhGfFa4IRLBA_GNlJTVc> .
@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:NP1267561.RAUTSZRS87XHPY4xtstMfCxaiBhGfFa4IRLBA_GNlJTVc130_head {
  this: np:hasAssertion dgn-np:NP1267561.RAUTSZRS87XHPY4xtstMfCxaiBhGfFa4IRLBA_GNlJTVc130_assertion;
    np:hasProvenance dgn-np:NP1267561.RAUTSZRS87XHPY4xtstMfCxaiBhGfFa4IRLBA_GNlJTVc130_provenance;
    np:hasPublicationInfo dgn-np:NP1267561.RAUTSZRS87XHPY4xtstMfCxaiBhGfFa4IRLBA_GNlJTVc130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1267561.RAUTSZRS87XHPY4xtstMfCxaiBhGfFa4IRLBA_GNlJTVc130_assertion a np:Assertion .
  
  dgn-np:NP1267561.RAUTSZRS87XHPY4xtstMfCxaiBhGfFa4IRLBA_GNlJTVc130_provenance a np:Provenance .
  
  dgn-np:NP1267561.RAUTSZRS87XHPY4xtstMfCxaiBhGfFa4IRLBA_GNlJTVc130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1267561.RAUTSZRS87XHPY4xtstMfCxaiBhGfFa4IRLBA_GNlJTVc130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGNdf537b60ffd3060c95ee60f9822395a1 sio:SIO_000628 miriam-gene:1080, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP1267561.RAUTSZRS87XHPY4xtstMfCxaiBhGfFa4IRLBA_GNlJTVc130_provenance {
  dgn-np:NP1267561.RAUTSZRS87XHPY4xtstMfCxaiBhGfFa4IRLBA_GNlJTVc130_assertion dcterms:description
      "[The underlying cause of cystic fibrosis (CF) is the loss of epithelial chloride and bicarbonate transport due to mutations in the CF transmembrane conductance regulator (CFTR) gene encoding the CFTR protein.]. 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:25732475;
    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:NP1267561.RAUTSZRS87XHPY4xtstMfCxaiBhGfFa4IRLBA_GNlJTVc130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:20+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" .
}