@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU> .
@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:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_head {
  this: np:hasAssertion dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_assertion;
    np:hasProvenance dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_provenance;
    np:hasPublicationInfo dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_assertion a np:Assertion .
  
  dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_provenance a np:Provenance .
  
  dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_assertion {
  miriam-gene:4287 a ncit:C16612 .
  
  lld:C0020179 a ncit:C7057 .
  
  dgn-gda:DGN4e04fb0afabe3ed30988c2286f8de9b1 sio:SIO_000628 miriam-gene:4287, lld:C0020179;
    a sio:SIO_001121 .
}

dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_provenance {
  dgn-np:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_assertion dcterms:description
      "[Clinical dysfunction as measured by the Scale for the Assessment and Rating of Ataxia (SARA) and the Unified Huntington's Disease Rating Scale functional assessment correlated best with the atrophy of pons in SCA1, with total brainstem atrophy in SCA3 and atrophy of total cerebellum in SCA6.]. 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:19631275;
    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:NP821373.RAeq3MoDN6Wf1IUzNrl5TAMvsZ2PEEuVFoWtXadzzfmwU130_publicationInfo {
  this: dcterms:created "2014-10-02T12:40:23+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" .
}