@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP574278.RA_bky45n2hSQbzR2tUaQTFuy2W96uhIX_dkOBLglg6Fk> .
@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:NP574278.RA_bky45n2hSQbzR2tUaQTFuy2W96uhIX_dkOBLglg6Fk130_head {
  this: np:hasAssertion dgn-np:NP574278.RA_bky45n2hSQbzR2tUaQTFuy2W96uhIX_dkOBLglg6Fk130_assertion;
    np:hasProvenance dgn-np:NP574278.RA_bky45n2hSQbzR2tUaQTFuy2W96uhIX_dkOBLglg6Fk130_provenance;
    np:hasPublicationInfo dgn-np:NP574278.RA_bky45n2hSQbzR2tUaQTFuy2W96uhIX_dkOBLglg6Fk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP574278.RA_bky45n2hSQbzR2tUaQTFuy2W96uhIX_dkOBLglg6Fk130_assertion a np:Assertion .
  
  dgn-np:NP574278.RA_bky45n2hSQbzR2tUaQTFuy2W96uhIX_dkOBLglg6Fk130_provenance a np:Provenance .
  
  dgn-np:NP574278.RA_bky45n2hSQbzR2tUaQTFuy2W96uhIX_dkOBLglg6Fk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP574278.RA_bky45n2hSQbzR2tUaQTFuy2W96uhIX_dkOBLglg6Fk130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0917713 a ncit:C7057 .
  
  dgn-gda:DGNbfcd8c493db8504dba2f5a42520ea3b3 sio:SIO_000628 miriam-gene:1756, lld:C0917713;
    a sio:SIO_001121 .
}

dgn-np:NP574278.RA_bky45n2hSQbzR2tUaQTFuy2W96uhIX_dkOBLglg6Fk130_provenance {
  dgn-np:NP574278.RA_bky45n2hSQbzR2tUaQTFuy2W96uhIX_dkOBLglg6Fk130_assertion dcterms:description
      "[In addition to a comprehensive assessment of muscular phenotypes that takes into account consequences of mutations on the expression of the dystrophin mRNA and protein, we provide and discuss genomic, mRNA, and protein data that pinpoint molecular mechanisms underlying BMD phenotypes associated with nonsense and frameshift mutations.]. 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:17041906;
    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:NP574278.RA_bky45n2hSQbzR2tUaQTFuy2W96uhIX_dkOBLglg6Fk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:46:05+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" .
}