@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP164123.RArSlFd2LJpvysqs14MH3JKfhZQjU3k8cuxbn4w9v9RYA> .
@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:NP164123.RArSlFd2LJpvysqs14MH3JKfhZQjU3k8cuxbn4w9v9RYA130_head {
  this: np:hasAssertion dgn-np:NP164123.RArSlFd2LJpvysqs14MH3JKfhZQjU3k8cuxbn4w9v9RYA130_assertion;
    np:hasProvenance dgn-np:NP164123.RArSlFd2LJpvysqs14MH3JKfhZQjU3k8cuxbn4w9v9RYA130_provenance;
    np:hasPublicationInfo dgn-np:NP164123.RArSlFd2LJpvysqs14MH3JKfhZQjU3k8cuxbn4w9v9RYA130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP164123.RArSlFd2LJpvysqs14MH3JKfhZQjU3k8cuxbn4w9v9RYA130_assertion a np:Assertion .
  
  dgn-np:NP164123.RArSlFd2LJpvysqs14MH3JKfhZQjU3k8cuxbn4w9v9RYA130_provenance a np:Provenance .
  
  dgn-np:NP164123.RArSlFd2LJpvysqs14MH3JKfhZQjU3k8cuxbn4w9v9RYA130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP164123.RArSlFd2LJpvysqs14MH3JKfhZQjU3k8cuxbn4w9v9RYA130_assertion {
  miriam-gene:1822 a ncit:C16612 .
  
  lld:C0087012 a ncit:C7057 .
  
  dgn-gda:DGNedfd369b0a1a60f77717ca67ab041f88 sio:SIO_000628 miriam-gene:1822, lld:C0087012;
    a sio:SIO_001121 .
}

dgn-np:NP164123.RArSlFd2LJpvysqs14MH3JKfhZQjU3k8cuxbn4w9v9RYA130_provenance {
  dgn-np:NP164123.RArSlFd2LJpvysqs14MH3JKfhZQjU3k8cuxbn4w9v9RYA130_assertion dcterms:description
      "[To identify various subtypes of spinocerebellar ataxias (SCAs) among 57 unrelated individuals clinically diagnosed as ataxia patients we analysed the SCA1, SCA2, SCA3, SCA6, SCA7 and DRPLA loci for expansion of CAG repeats.]. 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:10942107;
    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:NP164123.RArSlFd2LJpvysqs14MH3JKfhZQjU3k8cuxbn4w9v9RYA130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:29+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" .
}