@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP515891.RAZnx8gFdCO0N3lma7ZuySSeVfk7msH4qM4tlIYfp5R8I> .
@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:NP515891.RAZnx8gFdCO0N3lma7ZuySSeVfk7msH4qM4tlIYfp5R8I130_head {
  this: np:hasAssertion dgn-np:NP515891.RAZnx8gFdCO0N3lma7ZuySSeVfk7msH4qM4tlIYfp5R8I130_assertion;
    np:hasProvenance dgn-np:NP515891.RAZnx8gFdCO0N3lma7ZuySSeVfk7msH4qM4tlIYfp5R8I130_provenance;
    np:hasPublicationInfo dgn-np:NP515891.RAZnx8gFdCO0N3lma7ZuySSeVfk7msH4qM4tlIYfp5R8I130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP515891.RAZnx8gFdCO0N3lma7ZuySSeVfk7msH4qM4tlIYfp5R8I130_assertion a np:Assertion .
  
  dgn-np:NP515891.RAZnx8gFdCO0N3lma7ZuySSeVfk7msH4qM4tlIYfp5R8I130_provenance a np:Provenance .
  
  dgn-np:NP515891.RAZnx8gFdCO0N3lma7ZuySSeVfk7msH4qM4tlIYfp5R8I130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP515891.RAZnx8gFdCO0N3lma7ZuySSeVfk7msH4qM4tlIYfp5R8I130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0013264 a ncit:C7057 .
  
  dgn-gda:DGNfadfae0d660961111173c9fe9dc60b4b sio:SIO_000628 miriam-gene:1756, lld:C0013264;
    a sio:SIO_001121 .
}

dgn-np:NP515891.RAZnx8gFdCO0N3lma7ZuySSeVfk7msH4qM4tlIYfp5R8I130_provenance {
  dgn-np:NP515891.RAZnx8gFdCO0N3lma7ZuySSeVfk7msH4qM4tlIYfp5R8I130_assertion dcterms:description
      "[Antisense oligodeoxynucleotide against the splicing enhancer sequence (SES) in exon 19 of the dystrophin gene have been shown to induce exon 19 skipping and promote the expression of internally deleted dystrophin by correcting the translational reading frame in the cultured Duchenne muscular dystrophy (DMD) myocytes with the deletion of exon 20.]. 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:16198206;
    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:NP515891.RAZnx8gFdCO0N3lma7ZuySSeVfk7msH4qM4tlIYfp5R8I130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:38+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" .
}