@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP693644.RAqKfsEyGV0XaPNEfPtC3VLMlZ0HTL4UqIvvkBmiNXkGI> .
@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:NP693644.RAqKfsEyGV0XaPNEfPtC3VLMlZ0HTL4UqIvvkBmiNXkGI130_head {
  this: np:hasAssertion dgn-np:NP693644.RAqKfsEyGV0XaPNEfPtC3VLMlZ0HTL4UqIvvkBmiNXkGI130_assertion;
    np:hasProvenance dgn-np:NP693644.RAqKfsEyGV0XaPNEfPtC3VLMlZ0HTL4UqIvvkBmiNXkGI130_provenance;
    np:hasPublicationInfo dgn-np:NP693644.RAqKfsEyGV0XaPNEfPtC3VLMlZ0HTL4UqIvvkBmiNXkGI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP693644.RAqKfsEyGV0XaPNEfPtC3VLMlZ0HTL4UqIvvkBmiNXkGI130_assertion a np:Assertion .
  
  dgn-np:NP693644.RAqKfsEyGV0XaPNEfPtC3VLMlZ0HTL4UqIvvkBmiNXkGI130_provenance a np:Provenance .
  
  dgn-np:NP693644.RAqKfsEyGV0XaPNEfPtC3VLMlZ0HTL4UqIvvkBmiNXkGI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP693644.RAqKfsEyGV0XaPNEfPtC3VLMlZ0HTL4UqIvvkBmiNXkGI130_assertion {
  miriam-gene:146 a ncit:C16612 .
  
  lld:C1283761 a ncit:C7057 .
  
  dgn-gda:DGN6035ec55ec60336ec649b941f2eafe23 sio:SIO_000628 miriam-gene:146, lld:C1283761;
    a sio:SIO_001121 .
}

dgn-np:NP693644.RAqKfsEyGV0XaPNEfPtC3VLMlZ0HTL4UqIvvkBmiNXkGI130_provenance {
  dgn-np:NP693644.RAqKfsEyGV0XaPNEfPtC3VLMlZ0HTL4UqIvvkBmiNXkGI130_assertion dcterms:description
      "[We predict that selective interference of VCP interaction(s) with aberrant protein or its ERAD function will be an effective therapeutic site to rescue functional misfolded protein in diseases like cystic fibrosis and alpha-1-trypsin deficiency.]. 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:18798739;
    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:NP693644.RAqKfsEyGV0XaPNEfPtC3VLMlZ0HTL4UqIvvkBmiNXkGI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:59+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" .
}