@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP311300.RAadqUIDSsrAuXbh4BZFyMyDM5NEw61T5tBVQui1aJbTk> .
@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/v3.0.0/void/> .

dgn-np:NP311300.RAadqUIDSsrAuXbh4BZFyMyDM5NEw61T5tBVQui1aJbTk130_head {
  this: np:hasAssertion dgn-np:NP311300.RAadqUIDSsrAuXbh4BZFyMyDM5NEw61T5tBVQui1aJbTk130_assertion;
    np:hasProvenance dgn-np:NP311300.RAadqUIDSsrAuXbh4BZFyMyDM5NEw61T5tBVQui1aJbTk130_provenance;
    np:hasPublicationInfo dgn-np:NP311300.RAadqUIDSsrAuXbh4BZFyMyDM5NEw61T5tBVQui1aJbTk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP311300.RAadqUIDSsrAuXbh4BZFyMyDM5NEw61T5tBVQui1aJbTk130_assertion a np:Assertion .
  
  dgn-np:NP311300.RAadqUIDSsrAuXbh4BZFyMyDM5NEw61T5tBVQui1aJbTk130_provenance a np:Provenance .
  
  dgn-np:NP311300.RAadqUIDSsrAuXbh4BZFyMyDM5NEw61T5tBVQui1aJbTk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP311300.RAadqUIDSsrAuXbh4BZFyMyDM5NEw61T5tBVQui1aJbTk130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0030293 a ncit:C7057 .
  
  dgn-gda:DGN1574c7d5f615eaa9e58bf07a7fb550a5 sio:SIO_000628 miriam-gene:1080, lld:C0030293;
    a sio:SIO_001121 .
}

dgn-np:NP311300.RAadqUIDSsrAuXbh4BZFyMyDM5NEw61T5tBVQui1aJbTk130_provenance {
  dgn-np:NP311300.RAadqUIDSsrAuXbh4BZFyMyDM5NEw61T5tBVQui1aJbTk130_assertion dcterms:description
      "[Cystic fibrosis (CF) is an autosomal recessive disease caused by mutations in the CF transmembrane conductance regulator (CFTR) gene that results in abnormal viscous mucoid secretions in multiple organs and whose main clinical features are pancreatic insufficiency and chronic endobronchial infection.]. 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:18506640;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP311300.RAadqUIDSsrAuXbh4BZFyMyDM5NEw61T5tBVQui1aJbTk130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:39+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}