@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP511756.RAp9kGuCNHCXOpS2Y1H2GxFc25SkRjG6ac92dPDO3QemI> .
@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:NP511756.RAp9kGuCNHCXOpS2Y1H2GxFc25SkRjG6ac92dPDO3QemI130_head {
  this: np:hasAssertion dgn-np:NP511756.RAp9kGuCNHCXOpS2Y1H2GxFc25SkRjG6ac92dPDO3QemI130_assertion;
    np:hasProvenance dgn-np:NP511756.RAp9kGuCNHCXOpS2Y1H2GxFc25SkRjG6ac92dPDO3QemI130_provenance;
    np:hasPublicationInfo dgn-np:NP511756.RAp9kGuCNHCXOpS2Y1H2GxFc25SkRjG6ac92dPDO3QemI130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP511756.RAp9kGuCNHCXOpS2Y1H2GxFc25SkRjG6ac92dPDO3QemI130_assertion a np:Assertion .
  
  dgn-np:NP511756.RAp9kGuCNHCXOpS2Y1H2GxFc25SkRjG6ac92dPDO3QemI130_provenance a np:Provenance .
  
  dgn-np:NP511756.RAp9kGuCNHCXOpS2Y1H2GxFc25SkRjG6ac92dPDO3QemI130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP511756.RAp9kGuCNHCXOpS2Y1H2GxFc25SkRjG6ac92dPDO3QemI130_assertion {
  miriam-gene:5521 a ncit:C16612 .
  
  lld:C0007758 a ncit:C7057 .
  
  dgn-gda:DGNf0461df9d2a602602623b3939938add8 sio:SIO_000628 miriam-gene:5521, lld:C0007758;
    a sio:SIO_001121 .
}

dgn-np:NP511756.RAp9kGuCNHCXOpS2Y1H2GxFc25SkRjG6ac92dPDO3QemI130_provenance {
  dgn-np:NP511756.RAp9kGuCNHCXOpS2Y1H2GxFc25SkRjG6ac92dPDO3QemI130_assertion dcterms:description
      "[Spinocerebellar ataxia type 12 (SCA12) is an autosomal dominant cerebellar ataxia associated with the expansion of an unstable CAG repeat in the 5' region of the PPP2R2B gene on chromosome 5q31-5q32.]. 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:16138911;
    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:NP511756.RAp9kGuCNHCXOpS2Y1H2GxFc25SkRjG6ac92dPDO3QemI130_publicationInfo {
  this: dcterms:created "2016-05-13T12:45:36+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" .
}