@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1131916.RAEPpxGJoQno-L2C1_6DtdeYm3YNKCDw-pxDlSGaDOpW4> .
@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:NP1131916.RAEPpxGJoQno-L2C1_6DtdeYm3YNKCDw-pxDlSGaDOpW4130_head {
  this: np:hasAssertion dgn-np:NP1131916.RAEPpxGJoQno-L2C1_6DtdeYm3YNKCDw-pxDlSGaDOpW4130_assertion;
    np:hasProvenance dgn-np:NP1131916.RAEPpxGJoQno-L2C1_6DtdeYm3YNKCDw-pxDlSGaDOpW4130_provenance;
    np:hasPublicationInfo dgn-np:NP1131916.RAEPpxGJoQno-L2C1_6DtdeYm3YNKCDw-pxDlSGaDOpW4130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1131916.RAEPpxGJoQno-L2C1_6DtdeYm3YNKCDw-pxDlSGaDOpW4130_assertion a np:Assertion .
  
  dgn-np:NP1131916.RAEPpxGJoQno-L2C1_6DtdeYm3YNKCDw-pxDlSGaDOpW4130_provenance a np:Provenance .
  
  dgn-np:NP1131916.RAEPpxGJoQno-L2C1_6DtdeYm3YNKCDw-pxDlSGaDOpW4130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1131916.RAEPpxGJoQno-L2C1_6DtdeYm3YNKCDw-pxDlSGaDOpW4130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0917713 a ncit:C7057 .
  
  dgn-gda:DGNb07814e895406ef1bbb15b820429f2a0 sio:SIO_000628 miriam-gene:1756, lld:C0917713;
    a sio:SIO_001121 .
}

dgn-np:NP1131916.RAEPpxGJoQno-L2C1_6DtdeYm3YNKCDw-pxDlSGaDOpW4130_provenance {
  dgn-np:NP1131916.RAEPpxGJoQno-L2C1_6DtdeYm3YNKCDw-pxDlSGaDOpW4130_assertion dcterms:description
      "[Duchenne muscular Dystrophy (DMD) is an inherited disease caused by mutations in the dystrophin gene that disrupt the open reading frame, while in frame mutations result in Becker muscular dystrophy (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:24282529;
    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:NP1131916.RAEPpxGJoQno-L2C1_6DtdeYm3YNKCDw-pxDlSGaDOpW4130_publicationInfo {
  this: dcterms:created "2016-05-13T12:50:19+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" .
}