@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP554629.RADtLGL6XUcdjbrJEIohbAKKXrAfBFxeQaLmJPzobIM1U> .
@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:NP554629.RADtLGL6XUcdjbrJEIohbAKKXrAfBFxeQaLmJPzobIM1U130_head {
  this: np:hasAssertion dgn-np:NP554629.RADtLGL6XUcdjbrJEIohbAKKXrAfBFxeQaLmJPzobIM1U130_assertion;
    np:hasProvenance dgn-np:NP554629.RADtLGL6XUcdjbrJEIohbAKKXrAfBFxeQaLmJPzobIM1U130_provenance;
    np:hasPublicationInfo dgn-np:NP554629.RADtLGL6XUcdjbrJEIohbAKKXrAfBFxeQaLmJPzobIM1U130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP554629.RADtLGL6XUcdjbrJEIohbAKKXrAfBFxeQaLmJPzobIM1U130_assertion a np:Assertion .
  
  dgn-np:NP554629.RADtLGL6XUcdjbrJEIohbAKKXrAfBFxeQaLmJPzobIM1U130_provenance a np:Provenance .
  
  dgn-np:NP554629.RADtLGL6XUcdjbrJEIohbAKKXrAfBFxeQaLmJPzobIM1U130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP554629.RADtLGL6XUcdjbrJEIohbAKKXrAfBFxeQaLmJPzobIM1U130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0001614 a ncit:C7057 .
  
  dgn-gda:DGNc6b67870195e8ecb335600a4b0594349 sio:SIO_000628 miriam-gene:367, lld:C0001614;
    a sio:SIO_001121 .
}

dgn-np:NP554629.RADtLGL6XUcdjbrJEIohbAKKXrAfBFxeQaLmJPzobIM1U130_provenance {
  dgn-np:NP554629.RADtLGL6XUcdjbrJEIohbAKKXrAfBFxeQaLmJPzobIM1U130_assertion dcterms:description
      "[Lack of significant tissue-specific somatic mosaicism in SBMA including the cerebellar cortex may suggest that CAG repeat expansion in the mutant androgen receptor gene is far more stable compared with that in DRPLA and MJD as well as those reported in Huntington's disease.]. 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:8926495;
    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:NP554629.RADtLGL6XUcdjbrJEIohbAKKXrAfBFxeQaLmJPzobIM1U130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:34+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" .
}