@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k> .
@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:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_head {
  this: np:hasAssertion dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_assertion;
    np:hasProvenance dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_provenance;
    np:hasPublicationInfo dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_assertion a np:Assertion .
  
  dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_provenance a np:Provenance .
  
  dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_assertion {
  miriam-gene:7439 a ncit:C16612 .
  
  lld:C0917713 a ncit:C7057 .
  
  dgn-gda:DGNafa15dd4031dc53bfb034cfcf9efbcd2 sio:SIO_000628 miriam-gene:7439, lld:C0917713;
    a sio:SIO_001121 .
}

dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_provenance {
  dgn-np:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_assertion dcterms:description
      "[The aim of this study was to identify point mutations in patients with Duchenne or Becker muscular dystrophy (DMD or BMD) who have no gross DNA rearrangements detectable by Southern blot analysis or multiplex exon amplification.]. 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:8257990;
    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:NP1336924.RAMJPolEgVF4D8WkszWSGXW9UOyQyxCOVmvNhjkF7xp2k130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:52+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" .
}