@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q> .
@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/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@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/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_head {
  this: np:hasAssertion dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_assertion;
    np:hasProvenance dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_provenance;
    np:hasPublicationInfo dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_assertion a np:Assertion .
  
  dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_provenance a np:Provenance .
  
  dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_assertion {
  miriam-gene:1756 a ncit:C16612 .
  
  lld:C0041408 a ncit:C7057 .
  
  dgn-gda:DGN1669f8cf038a888fd80edfbda7eba94f sio:SIO_000628 miriam-gene:1756, lld:C0041408;
    a sio:SIO_001121 .
}

dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_provenance {
  dgn-np:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_assertion dcterms:description
      "[Neither female Duchenne muscular dystrophy (DMD) nor BMD due to homozygous dystrophin mutation has ever been identified although female DMD has been found in patients with Turner syndrome or unilateral parental disomy for X chromosome.]. 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:19396825;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^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:NP764204.RAkapC0CwtfSnJTA1_46b7OLwcarTn8llPlg9_BcFck9Q130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:42+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:disgenetrdf;
    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 "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}