@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP250188.RAv7TifsJUVf7zLubXo5jx5G5N020mbbIVXhiZfAQ3TPs> .
@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/v3.0.0/void/> .

dgn-np:NP250188.RAv7TifsJUVf7zLubXo5jx5G5N020mbbIVXhiZfAQ3TPs130_head {
  this: np:hasAssertion dgn-np:NP250188.RAv7TifsJUVf7zLubXo5jx5G5N020mbbIVXhiZfAQ3TPs130_assertion;
    np:hasProvenance dgn-np:NP250188.RAv7TifsJUVf7zLubXo5jx5G5N020mbbIVXhiZfAQ3TPs130_provenance;
    np:hasPublicationInfo dgn-np:NP250188.RAv7TifsJUVf7zLubXo5jx5G5N020mbbIVXhiZfAQ3TPs130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP250188.RAv7TifsJUVf7zLubXo5jx5G5N020mbbIVXhiZfAQ3TPs130_assertion a np:Assertion .
  
  dgn-np:NP250188.RAv7TifsJUVf7zLubXo5jx5G5N020mbbIVXhiZfAQ3TPs130_provenance a np:Provenance .
  
  dgn-np:NP250188.RAv7TifsJUVf7zLubXo5jx5G5N020mbbIVXhiZfAQ3TPs130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP250188.RAv7TifsJUVf7zLubXo5jx5G5N020mbbIVXhiZfAQ3TPs130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0026850 a ncit:C7057 .
  
  dgn-gda:DGN22d432f31d88c7e69fc98b632c89fa87 sio:SIO_000628 miriam-gene:367, lld:C0026850;
    a sio:SIO_001121 .
}

dgn-np:NP250188.RAv7TifsJUVf7zLubXo5jx5G5N020mbbIVXhiZfAQ3TPs130_provenance {
  dgn-np:NP250188.RAv7TifsJUVf7zLubXo5jx5G5N020mbbIVXhiZfAQ3TPs130_assertion dcterms:description
      "[We studied X inactivation patterns in manifesting carriers of familial and sporadic Duchenne muscular dystrophy (DMD) or unaffected carriers of DMD by analysis of the methylation of HpaII sites in the first exon of the human androgen-receptor gene (HUMARA) from peripheral blood samples.]. 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:9611069;
    prov:wasDerivedFrom dgn-void:befree-20150227;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP250188.RAv7TifsJUVf7zLubXo5jx5G5N020mbbIVXhiZfAQ3TPs130_publicationInfo {
  this: dcterms:created "2015-08-25T14:40:02+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 "v3.0.0.0" .
  
  dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}