@prefix dc: <http://purl.org/dc/terms/> .
@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP371059.RAChdWzO0P6AsjE19EUL-yMEeSn0KTUYBTN9HWGbuIM2A> .
@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 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:NP371059.RAChdWzO0P6AsjE19EUL-yMEeSn0KTUYBTN9HWGbuIM2A130_head {
  this: np:hasAssertion dgn-np:NP371059.RAChdWzO0P6AsjE19EUL-yMEeSn0KTUYBTN9HWGbuIM2A130_assertion;
    np:hasProvenance dgn-np:NP371059.RAChdWzO0P6AsjE19EUL-yMEeSn0KTUYBTN9HWGbuIM2A130_provenance;
    np:hasPublicationInfo dgn-np:NP371059.RAChdWzO0P6AsjE19EUL-yMEeSn0KTUYBTN9HWGbuIM2A130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP371059.RAChdWzO0P6AsjE19EUL-yMEeSn0KTUYBTN9HWGbuIM2A130_assertion a np:Assertion .
  
  dgn-np:NP371059.RAChdWzO0P6AsjE19EUL-yMEeSn0KTUYBTN9HWGbuIM2A130_provenance a np:Provenance .
  
  dgn-np:NP371059.RAChdWzO0P6AsjE19EUL-yMEeSn0KTUYBTN9HWGbuIM2A130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP371059.RAChdWzO0P6AsjE19EUL-yMEeSn0KTUYBTN9HWGbuIM2A130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0023895 a ncit:C7057 .
  
  dgn-gda:DGNafd9385e560f3c82b5912cccdc2f8615 sio:SIO_000628 miriam-gene:1080, lld:C0023895;
    a sio:SIO_001121 .
}

dgn-np:NP371059.RAChdWzO0P6AsjE19EUL-yMEeSn0KTUYBTN9HWGbuIM2A130_provenance {
  dgn-np:NP371059.RAChdWzO0P6AsjE19EUL-yMEeSn0KTUYBTN9HWGbuIM2A130_assertion dc:description
      "[To define risk factors for the development of liver disease associated with cystic fibrosis, we evaluated the possible role of specific mutations of the CFTR (cystic fibrosis transmembrane regulator) gene and of different clinical and demographic characteristics (sex, pancreatic status, meconium ileus or its equivalent) through a comparison of patients with cystic fibrosis and overt liver disease (n = 34) and those without liver disease (n = 155).]. 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:8120708;
    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:NP371059.RAChdWzO0P6AsjE19EUL-yMEeSn0KTUYBTN9HWGbuIM2A130_publicationInfo {
  this: dc:created "2014-10-02T12:35:37+02:00"^^xsd:dateTime;
    dc:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dc:rightsHolder dgn-void:IBIGroup;
    dc: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" .
}