@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP808934.RATEA0aH0rd-XmJAnLCoSnuP5wKst2xUBycIi_lgJXK2w> .
@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:NP808934.RATEA0aH0rd-XmJAnLCoSnuP5wKst2xUBycIi_lgJXK2w130_head {
  this: np:hasAssertion dgn-np:NP808934.RATEA0aH0rd-XmJAnLCoSnuP5wKst2xUBycIi_lgJXK2w130_assertion;
    np:hasProvenance dgn-np:NP808934.RATEA0aH0rd-XmJAnLCoSnuP5wKst2xUBycIi_lgJXK2w130_provenance;
    np:hasPublicationInfo dgn-np:NP808934.RATEA0aH0rd-XmJAnLCoSnuP5wKst2xUBycIi_lgJXK2w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP808934.RATEA0aH0rd-XmJAnLCoSnuP5wKst2xUBycIi_lgJXK2w130_assertion a np:Assertion .
  
  dgn-np:NP808934.RATEA0aH0rd-XmJAnLCoSnuP5wKst2xUBycIi_lgJXK2w130_provenance a np:Provenance .
  
  dgn-np:NP808934.RATEA0aH0rd-XmJAnLCoSnuP5wKst2xUBycIi_lgJXK2w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP808934.RATEA0aH0rd-XmJAnLCoSnuP5wKst2xUBycIi_lgJXK2w130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0393547 a ncit:C7057 .
  
  dgn-gda:DGN21486731a4068c9955405248610b911a sio:SIO_000628 miriam-gene:367, lld:C0393547;
    a sio:SIO_001121 .
}

dgn-np:NP808934.RATEA0aH0rd-XmJAnLCoSnuP5wKst2xUBycIi_lgJXK2w130_provenance {
  dgn-np:NP808934.RATEA0aH0rd-XmJAnLCoSnuP5wKst2xUBycIi_lgJXK2w130_assertion dcterms:description
      "[In Kennedy's syndrome, a mutation in the androgen receptor (AR) gene leads to sensory and lower motor neurone degeneration, therefore genes that are regulated by androgens in neurones may be important in the process of motor neurone cell death.]. 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:7595605;
    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:NP808934.RATEA0aH0rd-XmJAnLCoSnuP5wKst2xUBycIi_lgJXK2w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:16+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" .
}