@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1137279.RAtbfnaxfP2dQatqNIzeWjjOiELX6E5vpGJkfWwKhKyrA> .
@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:NP1137279.RAtbfnaxfP2dQatqNIzeWjjOiELX6E5vpGJkfWwKhKyrA130_head {
  this: np:hasAssertion dgn-np:NP1137279.RAtbfnaxfP2dQatqNIzeWjjOiELX6E5vpGJkfWwKhKyrA130_assertion;
    np:hasProvenance dgn-np:NP1137279.RAtbfnaxfP2dQatqNIzeWjjOiELX6E5vpGJkfWwKhKyrA130_provenance;
    np:hasPublicationInfo dgn-np:NP1137279.RAtbfnaxfP2dQatqNIzeWjjOiELX6E5vpGJkfWwKhKyrA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1137279.RAtbfnaxfP2dQatqNIzeWjjOiELX6E5vpGJkfWwKhKyrA130_assertion a np:Assertion .
  
  dgn-np:NP1137279.RAtbfnaxfP2dQatqNIzeWjjOiELX6E5vpGJkfWwKhKyrA130_provenance a np:Provenance .
  
  dgn-np:NP1137279.RAtbfnaxfP2dQatqNIzeWjjOiELX6E5vpGJkfWwKhKyrA130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1137279.RAtbfnaxfP2dQatqNIzeWjjOiELX6E5vpGJkfWwKhKyrA130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGN73f533d016bbeb65915e6707bfd5f544 sio:SIO_000628 miriam-gene:1080, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP1137279.RAtbfnaxfP2dQatqNIzeWjjOiELX6E5vpGJkfWwKhKyrA130_provenance {
  dgn-np:NP1137279.RAtbfnaxfP2dQatqNIzeWjjOiELX6E5vpGJkfWwKhKyrA130_assertion dcterms:description
      "[Mutations in this gene affect organs with exocrine functions and the main cause of morbidity and mortality for CF patients is the lung pathology in which the defect in CFTR decreases chloride secretion, lowering the airway surface liquid height and increasing mucus viscosity.]. 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:24342234;
    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:NP1137279.RAtbfnaxfP2dQatqNIzeWjjOiELX6E5vpGJkfWwKhKyrA130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:21+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" .
}