@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP326167.RAQs0urjE-Iz90NHf9Qc4GiL8OIWSDhAnvfBK3xi6so30> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .
dgn-np:NP326167.RAQs0urjE-Iz90NHf9Qc4GiL8OIWSDhAnvfBK3xi6so30130_head {
  this: np:hasAssertion dgn-np:NP326167.RAQs0urjE-Iz90NHf9Qc4GiL8OIWSDhAnvfBK3xi6so30130_assertion ;
    np:hasProvenance dgn-np:NP326167.RAQs0urjE-Iz90NHf9Qc4GiL8OIWSDhAnvfBK3xi6so30130_provenance ;
    np:hasPublicationInfo dgn-np:NP326167.RAQs0urjE-Iz90NHf9Qc4GiL8OIWSDhAnvfBK3xi6so30130_publicationInfo ;
    a np:Nanopublication .
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  dgn-np:NP326167.RAQs0urjE-Iz90NHf9Qc4GiL8OIWSDhAnvfBK3xi6so30130_provenance a np:Provenance .
  dgn-np:NP326167.RAQs0urjE-Iz90NHf9Qc4GiL8OIWSDhAnvfBK3xi6so30130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP326167.RAQs0urjE-Iz90NHf9Qc4GiL8OIWSDhAnvfBK3xi6so30130_assertion {
  miriam-gene:1080 a ncit:C16612 .
  lld:C0011847 a ncit:C7057 .
  dgn-gda:DGN430ac65c51f400cf9d5685a8f79d627a sio:SIO_000628 miriam-gene:1080 , lld:C0011847 ;
    a sio:SIO_001121 .
}
dgn-np:NP326167.RAQs0urjE-Iz90NHf9Qc4GiL8OIWSDhAnvfBK3xi6so30130_provenance {
  dgn-np:NP326167.RAQs0urjE-Iz90NHf9Qc4GiL8OIWSDhAnvfBK3xi6so30130_assertion dcterms:description "[The proposed mechanism is supported by several pieces of evidence including: (1) the absolute essentiality of an intact unfolded protein response (UPR) machinery for survival of pancreatic beta-cells, (2) the high susceptibility of beta-cells to prolonged ER stress leading to induction of pro-apoptotic factors and apoptosis pathways in beta-cells, (3) CF patients with mutations in CFTR gene that are engaging the ER quality control system (ERAD) and hence UPR signalling are twenty time more likely to develop diabetes than those with other types of CF-causing mutations, and (4) the high levels of CFTR gene expression in pancreatic islet cells.]. 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:18851900 ;
    prov:wasDerivedFrom dgn-void:befree-20140225 ;
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  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:NP326167.RAQs0urjE-Iz90NHf9Qc4GiL8OIWSDhAnvfBK3xi6so30130_publicationInfo {
  this: dcterms:created "2014-10-02T12:35:10+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:disgenetrdf ;
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