@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP741286.RAhJ5kvBbfyd60albODOKnDHBeZhJEz8l9Nqt1H61waY0> .
@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:NP741286.RAhJ5kvBbfyd60albODOKnDHBeZhJEz8l9Nqt1H61waY0130_head {
  this: np:hasAssertion dgn-np:NP741286.RAhJ5kvBbfyd60albODOKnDHBeZhJEz8l9Nqt1H61waY0130_assertion;
    np:hasProvenance dgn-np:NP741286.RAhJ5kvBbfyd60albODOKnDHBeZhJEz8l9Nqt1H61waY0130_provenance;
    np:hasPublicationInfo dgn-np:NP741286.RAhJ5kvBbfyd60albODOKnDHBeZhJEz8l9Nqt1H61waY0130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP741286.RAhJ5kvBbfyd60albODOKnDHBeZhJEz8l9Nqt1H61waY0130_assertion a np:Assertion .
  
  dgn-np:NP741286.RAhJ5kvBbfyd60albODOKnDHBeZhJEz8l9Nqt1H61waY0130_provenance a np:Provenance .
  
  dgn-np:NP741286.RAhJ5kvBbfyd60albODOKnDHBeZhJEz8l9Nqt1H61waY0130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP741286.RAhJ5kvBbfyd60albODOKnDHBeZhJEz8l9Nqt1H61waY0130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0026850 a ncit:C7057 .
  
  dgn-gda:DGN839f8140d1d4cf0da4860935455d4fff sio:SIO_000628 miriam-gene:1756, lld:C0026850;
    a sio:SIO_001121 .
}

dgn-np:NP741286.RAhJ5kvBbfyd60albODOKnDHBeZhJEz8l9Nqt1H61waY0130_provenance {
  dgn-np:NP741286.RAhJ5kvBbfyd60albODOKnDHBeZhJEz8l9Nqt1H61waY0130_assertion dcterms:description
      "[Currently, multiplex ligation-dependent probe amplification (MLPA) has been recognized as the most powerful and convenient method to identify exon deletions or duplications in the dystrophin gene, the mutation of which causes Duchenne and Becker muscular dystrophies (DMD/BMD).]. 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:19473085;
    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:NP741286.RAhJ5kvBbfyd60albODOKnDHBeZhJEz8l9Nqt1H61waY0130_publicationInfo {
  this: dcterms:created "2016-05-13T12:47:21+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" .
}