@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP248838.RAaTvCwVGa9OqCZgI7uUqiI7UEMPRljmJ1xyUsmbcf7c0> .
@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:NP248838.RAaTvCwVGa9OqCZgI7uUqiI7UEMPRljmJ1xyUsmbcf7c0130_head {
  this: np:hasAssertion dgn-np:NP248838.RAaTvCwVGa9OqCZgI7uUqiI7UEMPRljmJ1xyUsmbcf7c0130_assertion;
    np:hasProvenance dgn-np:NP248838.RAaTvCwVGa9OqCZgI7uUqiI7UEMPRljmJ1xyUsmbcf7c0130_provenance;
    np:hasPublicationInfo dgn-np:NP248838.RAaTvCwVGa9OqCZgI7uUqiI7UEMPRljmJ1xyUsmbcf7c0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP248838.RAaTvCwVGa9OqCZgI7uUqiI7UEMPRljmJ1xyUsmbcf7c0130_assertion a np:Assertion .
  
  dgn-np:NP248838.RAaTvCwVGa9OqCZgI7uUqiI7UEMPRljmJ1xyUsmbcf7c0130_provenance a np:Provenance .
  
  dgn-np:NP248838.RAaTvCwVGa9OqCZgI7uUqiI7UEMPRljmJ1xyUsmbcf7c0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP248838.RAaTvCwVGa9OqCZgI7uUqiI7UEMPRljmJ1xyUsmbcf7c0130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0026846 a ncit:C7057 .
  
  dgn-gda:DGN8fbb980c645073c496beeef7a8964d80 sio:SIO_000628 miriam-gene:1756, lld:C0026846;
    a sio:SIO_001121 .
}

dgn-np:NP248838.RAaTvCwVGa9OqCZgI7uUqiI7UEMPRljmJ1xyUsmbcf7c0130_provenance {
  dgn-np:NP248838.RAaTvCwVGa9OqCZgI7uUqiI7UEMPRljmJ1xyUsmbcf7c0130_assertion dcterms:description
      "[Out of three mutations in the dystrophin gene that cause Duchenne muscular dystrophy (DMD), the most common, serious childhood muscle wasting disease, two are genomic deletions of one or more exons that disrupt the reading frame.]. 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:18570328;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP248838.RAaTvCwVGa9OqCZgI7uUqiI7UEMPRljmJ1xyUsmbcf7c0130_publicationInfo {
  this: dcterms:created "2014-10-02T12:34:19+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;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}