@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP213470.RAQFz4Gzay1wRSIJBWmdKkELoAtYAj6Y4lMDu4Yfkk4mQ> .
@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:NP213470.RAQFz4Gzay1wRSIJBWmdKkELoAtYAj6Y4lMDu4Yfkk4mQ130_head {
  this: np:hasAssertion dgn-np:NP213470.RAQFz4Gzay1wRSIJBWmdKkELoAtYAj6Y4lMDu4Yfkk4mQ130_assertion;
    np:hasProvenance dgn-np:NP213470.RAQFz4Gzay1wRSIJBWmdKkELoAtYAj6Y4lMDu4Yfkk4mQ130_provenance;
    np:hasPublicationInfo dgn-np:NP213470.RAQFz4Gzay1wRSIJBWmdKkELoAtYAj6Y4lMDu4Yfkk4mQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP213470.RAQFz4Gzay1wRSIJBWmdKkELoAtYAj6Y4lMDu4Yfkk4mQ130_assertion a np:Assertion .
  
  dgn-np:NP213470.RAQFz4Gzay1wRSIJBWmdKkELoAtYAj6Y4lMDu4Yfkk4mQ130_provenance a np:Provenance .
  
  dgn-np:NP213470.RAQFz4Gzay1wRSIJBWmdKkELoAtYAj6Y4lMDu4Yfkk4mQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP213470.RAQFz4Gzay1wRSIJBWmdKkELoAtYAj6Y4lMDu4Yfkk4mQ130_assertion {
  miriam-gene:23064 a ncit:C16612 .
  
  lld:C0004134 a ncit:C7057 .
  
  dgn-gda:DGN95eef9775e7fce772493757516bad20b sio:SIO_000628 miriam-gene:23064, lld:C0004134;
    a sio:SIO_001121 .
}

dgn-np:NP213470.RAQFz4Gzay1wRSIJBWmdKkELoAtYAj6Y4lMDu4Yfkk4mQ130_provenance {
  dgn-np:NP213470.RAQFz4Gzay1wRSIJBWmdKkELoAtYAj6Y4lMDu4Yfkk4mQ130_assertion dcterms:description
      "[We analysed the phenotypic spectrum of 19 AOA2 patients with mutations in SETX, which seems to be the third most frequent form of ARCA in Algeria after Freidreich ataxia and Ataxia with vitamin E deficiency.]. 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:19141356;
    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:NP213470.RAQFz4Gzay1wRSIJBWmdKkELoAtYAj6Y4lMDu4Yfkk4mQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:58+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" .
}