@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI> .
@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:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_head {
  this: np:hasAssertion dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_assertion;
    np:hasProvenance dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_provenance;
    np:hasPublicationInfo dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_assertion a np:Assertion .
  
  dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_provenance a np:Provenance .
  
  dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGN29b69132d22aaaccc62743e96d332c54 sio:SIO_000628 miriam-gene:1080, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_provenance {
  dgn-np:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_assertion dcterms:description
      "[Cystic fibrosis, the most common lethal genetic disease affecting young people in North America, is caused by failure of the chloride ion channel known as CFTR (cystic fibrosis transmembrane conductance regulator).]. 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:25367045;
    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:NP1234641.RA9PTV8o5lOr_2ch1_TAOEmhqN87I30wv90PYRLbXh1tI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:05+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" .
}