@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP848216.RA6Q9phFe2CQU2XYz_NP_tgsDGRUk62KfHTKQqbF0sbLs> .
@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:NP848216.RA6Q9phFe2CQU2XYz_NP_tgsDGRUk62KfHTKQqbF0sbLs130_head {
  this: np:hasAssertion dgn-np:NP848216.RA6Q9phFe2CQU2XYz_NP_tgsDGRUk62KfHTKQqbF0sbLs130_assertion;
    np:hasProvenance dgn-np:NP848216.RA6Q9phFe2CQU2XYz_NP_tgsDGRUk62KfHTKQqbF0sbLs130_provenance;
    np:hasPublicationInfo dgn-np:NP848216.RA6Q9phFe2CQU2XYz_NP_tgsDGRUk62KfHTKQqbF0sbLs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP848216.RA6Q9phFe2CQU2XYz_NP_tgsDGRUk62KfHTKQqbF0sbLs130_assertion a np:Assertion .
  
  dgn-np:NP848216.RA6Q9phFe2CQU2XYz_NP_tgsDGRUk62KfHTKQqbF0sbLs130_provenance a np:Provenance .
  
  dgn-np:NP848216.RA6Q9phFe2CQU2XYz_NP_tgsDGRUk62KfHTKQqbF0sbLs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP848216.RA6Q9phFe2CQU2XYz_NP_tgsDGRUk62KfHTKQqbF0sbLs130_assertion {
  miriam-gene:10598 a ncit:C16612 .
  
  lld:C0019247 a ncit:C7057 .
  
  dgn-gda:DGNf4746f95fc04db6fbd48463f344e1b0f sio:SIO_000628 miriam-gene:10598, lld:C0019247;
    a sio:SIO_001122 .
}

dgn-np:NP848216.RA6Q9phFe2CQU2XYz_NP_tgsDGRUk62KfHTKQqbF0sbLs130_provenance {
  dgn-np:NP848216.RA6Q9phFe2CQU2XYz_NP_tgsDGRUk62KfHTKQqbF0sbLs130_assertion dcterms:description
      "[Mutations in both the N- and C-terminal domains of Aha1 impair its ability to bind Hsp90 and stimulate its ATPase activity in vitro and impair in vivo the ability of the Hsp90 system to modulate the folding and trafficking of wild-type and variant (DeltaF508) cystic fibrosis transmembrane conductance regulator (CFTR) responsible for the inherited disease cystic fibrosis (CF).]. 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:20089831;
    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:NP848216.RA6Q9phFe2CQU2XYz_NP_tgsDGRUk62KfHTKQqbF0sbLs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:46:15+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" .
}