@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP358385.RANE6U-u8ODNPurhSlDov1K_5Prn5BGn4ZpH9EupZt_fk> .
@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:NP358385.RANE6U-u8ODNPurhSlDov1K_5Prn5BGn4ZpH9EupZt_fk130_head {
  this: np:hasAssertion dgn-np:NP358385.RANE6U-u8ODNPurhSlDov1K_5Prn5BGn4ZpH9EupZt_fk130_assertion;
    np:hasProvenance dgn-np:NP358385.RANE6U-u8ODNPurhSlDov1K_5Prn5BGn4ZpH9EupZt_fk130_provenance;
    np:hasPublicationInfo dgn-np:NP358385.RANE6U-u8ODNPurhSlDov1K_5Prn5BGn4ZpH9EupZt_fk130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP358385.RANE6U-u8ODNPurhSlDov1K_5Prn5BGn4ZpH9EupZt_fk130_assertion a np:Assertion .
  
  dgn-np:NP358385.RANE6U-u8ODNPurhSlDov1K_5Prn5BGn4ZpH9EupZt_fk130_provenance a np:Provenance .
  
  dgn-np:NP358385.RANE6U-u8ODNPurhSlDov1K_5Prn5BGn4ZpH9EupZt_fk130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP358385.RANE6U-u8ODNPurhSlDov1K_5Prn5BGn4ZpH9EupZt_fk130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0917713 a ncit:C7057 .
  
  dgn-gda:DGN5eb130413ec8aeec02739fd2a7ac960c sio:SIO_000628 miriam-gene:1756, lld:C0917713;
    a sio:SIO_001121 .
}

dgn-np:NP358385.RANE6U-u8ODNPurhSlDov1K_5Prn5BGn4ZpH9EupZt_fk130_provenance {
  dgn-np:NP358385.RANE6U-u8ODNPurhSlDov1K_5Prn5BGn4ZpH9EupZt_fk130_assertion dcterms:description
      "[Deletions and point mutations in the dystrophin gene cause either the severe progressive myopathy Duchenne muscular dystrophy (DMD) or the milder Becker muscular dystrophy, depending on whether the translational reading frame is lost or maintained.]. 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:12077324;
    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:NP358385.RANE6U-u8ODNPurhSlDov1K_5Prn5BGn4ZpH9EupZt_fk130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:27+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" .
}