@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP337131.RAurP7Jj8C1obe5Ytc536CQwreBR2qrtIvKlSwSt1RZQY> .
@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:NP337131.RAurP7Jj8C1obe5Ytc536CQwreBR2qrtIvKlSwSt1RZQY130_head {
  this: np:hasAssertion dgn-np:NP337131.RAurP7Jj8C1obe5Ytc536CQwreBR2qrtIvKlSwSt1RZQY130_assertion;
    np:hasProvenance dgn-np:NP337131.RAurP7Jj8C1obe5Ytc536CQwreBR2qrtIvKlSwSt1RZQY130_provenance;
    np:hasPublicationInfo dgn-np:NP337131.RAurP7Jj8C1obe5Ytc536CQwreBR2qrtIvKlSwSt1RZQY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP337131.RAurP7Jj8C1obe5Ytc536CQwreBR2qrtIvKlSwSt1RZQY130_assertion a np:Assertion .
  
  dgn-np:NP337131.RAurP7Jj8C1obe5Ytc536CQwreBR2qrtIvKlSwSt1RZQY130_provenance a np:Provenance .
  
  dgn-np:NP337131.RAurP7Jj8C1obe5Ytc536CQwreBR2qrtIvKlSwSt1RZQY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP337131.RAurP7Jj8C1obe5Ytc536CQwreBR2qrtIvKlSwSt1RZQY130_assertion {
  miriam-gene:367 a ncit:C16612 .
  
  lld:C0002736 a ncit:C7057 .
  
  dgn-gda:DGN8f4cf64e695861b7e258a1c9720f78fb sio:SIO_000628 miriam-gene:367, lld:C0002736;
    a sio:SIO_001121 .
}

dgn-np:NP337131.RAurP7Jj8C1obe5Ytc536CQwreBR2qrtIvKlSwSt1RZQY130_provenance {
  dgn-np:NP337131.RAurP7Jj8C1obe5Ytc536CQwreBR2qrtIvKlSwSt1RZQY130_assertion dcterms:description
      "[Secondly, cytoskeletal function may be impaired in both diseases as decreased transactivational activity of expanded androgen receptor may cause an abnormal pattern of tubulin expression in motor neurons in Kennedy's disease and disruption of neurofilament organisation is a hallmark of amyotrophic lateral sclerosis.]. 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:11719252;
    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:NP337131.RAurP7Jj8C1obe5Ytc536CQwreBR2qrtIvKlSwSt1RZQY130_publicationInfo {
  this: dcterms:created "2016-05-13T12:44:18+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" .
}