@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI> .
@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:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_head {
  this: np:hasAssertion dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_assertion;
    np:hasProvenance dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_provenance;
    np:hasPublicationInfo dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_assertion a np:Assertion .
  
  dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_provenance a np:Provenance .
  
  dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0013264 a ncit:C7057 .
  
  dgn-gda:DGN932585718db22ce1f5b12f8883612a7a sio:SIO_000628 miriam-gene:1756, lld:C0013264;
    a sio:SIO_001121 .
}

dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_provenance {
  dgn-np:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_assertion dcterms:description
      "[A deeper understanding of the events arising as an early consequence of dystrophin deficiency in these two situations may strengthen approaches to therapy for DMD designed to improve muscle function and the quality of life.]. 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:18327663;
    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:NP154827.RA2jMqwiLZISIwURM5KLtJOnTp741bJLUz466QdZAWUJI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:22+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" .
}