@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP350688.RA0tt1yuyORvDaYsFNamlEonh4hYyK46qVUftDescGI-g> .
@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:NP350688.RA0tt1yuyORvDaYsFNamlEonh4hYyK46qVUftDescGI-g130_head {
  this: np:hasAssertion dgn-np:NP350688.RA0tt1yuyORvDaYsFNamlEonh4hYyK46qVUftDescGI-g130_assertion;
    np:hasProvenance dgn-np:NP350688.RA0tt1yuyORvDaYsFNamlEonh4hYyK46qVUftDescGI-g130_provenance;
    np:hasPublicationInfo dgn-np:NP350688.RA0tt1yuyORvDaYsFNamlEonh4hYyK46qVUftDescGI-g130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP350688.RA0tt1yuyORvDaYsFNamlEonh4hYyK46qVUftDescGI-g130_assertion a np:Assertion .
  
  dgn-np:NP350688.RA0tt1yuyORvDaYsFNamlEonh4hYyK46qVUftDescGI-g130_provenance a np:Provenance .
  
  dgn-np:NP350688.RA0tt1yuyORvDaYsFNamlEonh4hYyK46qVUftDescGI-g130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP350688.RA0tt1yuyORvDaYsFNamlEonh4hYyK46qVUftDescGI-g130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGN910e8433f623e8439875852d11cc6dc5 sio:SIO_000628 miriam-gene:1080, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP350688.RA0tt1yuyORvDaYsFNamlEonh4hYyK46qVUftDescGI-g130_provenance {
  dgn-np:NP350688.RA0tt1yuyORvDaYsFNamlEonh4hYyK46qVUftDescGI-g130_assertion dcterms:description
      "[While originally characterized as a collection of related syndromes, cystic fibrosis (CF) is now recognized as a single disease whose diverse symptoms stem from the wide tissue distribution of the gene product that is defective in CF, the ion channel and regulator, cystic fibrosis transmembrane conductance regulator (CFTR).]. 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:11932230;
    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:NP350688.RA0tt1yuyORvDaYsFNamlEonh4hYyK46qVUftDescGI-g130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:24+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" .
}