@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP739015.RAviHxMzds4xc3V2EH8sGDdcrAaLlQr82BpmPojUbB25Y> .
@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:NP739015.RAviHxMzds4xc3V2EH8sGDdcrAaLlQr82BpmPojUbB25Y130_head {
  this: np:hasAssertion dgn-np:NP739015.RAviHxMzds4xc3V2EH8sGDdcrAaLlQr82BpmPojUbB25Y130_assertion;
    np:hasProvenance dgn-np:NP739015.RAviHxMzds4xc3V2EH8sGDdcrAaLlQr82BpmPojUbB25Y130_provenance;
    np:hasPublicationInfo dgn-np:NP739015.RAviHxMzds4xc3V2EH8sGDdcrAaLlQr82BpmPojUbB25Y130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP739015.RAviHxMzds4xc3V2EH8sGDdcrAaLlQr82BpmPojUbB25Y130_assertion a np:Assertion .
  
  dgn-np:NP739015.RAviHxMzds4xc3V2EH8sGDdcrAaLlQr82BpmPojUbB25Y130_provenance a np:Provenance .
  
  dgn-np:NP739015.RAviHxMzds4xc3V2EH8sGDdcrAaLlQr82BpmPojUbB25Y130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP739015.RAviHxMzds4xc3V2EH8sGDdcrAaLlQr82BpmPojUbB25Y130_assertion {
  miriam-gene:4864 a ncit:C16612 .
  
  lld:C0033300 a ncit:C7057 .
  
  dgn-gda:DGNa5033fd55c1e7e1cd2ad05225608e806 sio:SIO_000628 miriam-gene:4864, lld:C0033300;
    a sio:SIO_001121 .
}

dgn-np:NP739015.RAviHxMzds4xc3V2EH8sGDdcrAaLlQr82BpmPojUbB25Y130_provenance {
  dgn-np:NP739015.RAviHxMzds4xc3V2EH8sGDdcrAaLlQr82BpmPojUbB25Y130_assertion dcterms:description
      "[Two mutants, causing prenatal skin disease restrictive dermopathy (RD) and the premature aging disease Hutchinson Gilford progeria syndrome, were used for expression in HeLa cells to investigate their impact on the subcellular localization of NPC-associated proteins and nuclear protein import.]. 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:19442658;
    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:NP739015.RAviHxMzds4xc3V2EH8sGDdcrAaLlQr82BpmPojUbB25Y130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:20+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" .
}