@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw> .
@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:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_head {
  this: np:hasAssertion dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_assertion;
    np:hasProvenance dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_provenance;
    np:hasPublicationInfo dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_assertion a np:Assertion .
  
  dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_provenance a np:Provenance .
  
  dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0747198 a ncit:C7057 .
  
  dgn-gda:DGN467ae336b7064b568c992fea9c662ec9 sio:SIO_000628 miriam-gene:1080, lld:C0747198;
    a sio:SIO_001121 .
}

dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_provenance {
  dgn-np:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_assertion dcterms:description
      "[Mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene are associated with different related disorders such as congenital bilateral absence of the vas deferens, chronic idiopathic pancreatitis, or disseminated bronchiectasis (DB).]. 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:12123489;
    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:NP361580.RAtqig6C1ndsxf-2COnFHhMjCkY7im0HmVZHFaqiwoRpw130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:29+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" .
}