@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0> .
@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:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_head {
  this: np:hasAssertion dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_assertion;
    np:hasProvenance dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_provenance;
    np:hasPublicationInfo dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_assertion a np:Assertion .
  
  dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_provenance a np:Provenance .
  
  dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  
  lld:C0010674 a ncit:C7057 .
  
  dgn-gda:DGN0bc94c0566f4f64e4686a01174b37473 sio:SIO_000628 miriam-gene:1080, lld:C0010674;
    a sio:SIO_001121 .
}

dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_provenance {
  dgn-np:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_assertion dcterms:description
      "[Cystic fibrosis (CF) is a common, fatal hereditary disease resulting from mutations of the human cystic fibrosis transmembrane conductance regulator (CFTR) gene in which epithelial cells throughout the body manifest altered regulation of apical membrane chloride secretion.]. 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:7948135;
    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:NP1327835.RASO9YljkbcUx1P3yH8nyLlYNm69qKdYma44SmpP6EZg0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:48+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" .
}