@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP355571.RAz6gOryXlFmIW3kkk4nExNE89Jj31teqjcPTFnPy_8rE> .
@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/v3.0.0/void/> .
dgn-np:NP355571.RAz6gOryXlFmIW3kkk4nExNE89Jj31teqjcPTFnPy_8rE130_head {
   this: np:hasAssertion dgn-np:NP355571.RAz6gOryXlFmIW3kkk4nExNE89Jj31teqjcPTFnPy_8rE130_assertion ;
    np:hasProvenance dgn-np:NP355571.RAz6gOryXlFmIW3kkk4nExNE89Jj31teqjcPTFnPy_8rE130_provenance ;
    np:hasPublicationInfo dgn-np:NP355571.RAz6gOryXlFmIW3kkk4nExNE89Jj31teqjcPTFnPy_8rE130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP355571.RAz6gOryXlFmIW3kkk4nExNE89Jj31teqjcPTFnPy_8rE130_assertion a np:Assertion .
  dgn-np:NP355571.RAz6gOryXlFmIW3kkk4nExNE89Jj31teqjcPTFnPy_8rE130_provenance a np:Provenance .
  dgn-np:NP355571.RAz6gOryXlFmIW3kkk4nExNE89Jj31teqjcPTFnPy_8rE130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP355571.RAz6gOryXlFmIW3kkk4nExNE89Jj31teqjcPTFnPy_8rE130_assertion {
   miriam-gene:1756 a ncit:C16612 .
  lld:C0679466 a ncit:C7057 .
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}
dgn-np:NP355571.RAz6gOryXlFmIW3kkk4nExNE89Jj31teqjcPTFnPy_8rE130_provenance {
   dgn-np:NP355571.RAz6gOryXlFmIW3kkk4nExNE89Jj31teqjcPTFnPy_8rE130_assertion dcterms:description "[Two decades of molecular, cellular, and functional studies considerably increased our understanding of dystrophins function and unveiled the complex etiology of the cognitive deficits in Duchenne muscular dystrophy (DMD), which involves altered expression of several dystrophin-gene products in brain.]. 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:20625423 ;
    prov:wasDerivedFrom dgn-void:befree-20150227 ;
    prov:wasGeneratedBy eco:ECO_0000203 .
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP355571.RAz6gOryXlFmIW3kkk4nExNE89Jj31teqjcPTFnPy_8rE130_publicationInfo {
   this: dcterms:created "2015-08-25T14:41:05+02:00"^^xsd:dateTime ;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/> ;
    dcterms:rightsHolder dgn-void:IBIGroup ;
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}