@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP892610.RA1S7R0Db_X2ubtaSzLmP2Jw3VBE63OnvyOgp13gBBfjw> .
@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:NP892610.RA1S7R0Db_X2ubtaSzLmP2Jw3VBE63OnvyOgp13gBBfjw130_head {
  this: np:hasAssertion dgn-np:NP892610.RA1S7R0Db_X2ubtaSzLmP2Jw3VBE63OnvyOgp13gBBfjw130_assertion;
    np:hasProvenance dgn-np:NP892610.RA1S7R0Db_X2ubtaSzLmP2Jw3VBE63OnvyOgp13gBBfjw130_provenance;
    np:hasPublicationInfo dgn-np:NP892610.RA1S7R0Db_X2ubtaSzLmP2Jw3VBE63OnvyOgp13gBBfjw130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP892610.RA1S7R0Db_X2ubtaSzLmP2Jw3VBE63OnvyOgp13gBBfjw130_assertion a np:Assertion .
  
  dgn-np:NP892610.RA1S7R0Db_X2ubtaSzLmP2Jw3VBE63OnvyOgp13gBBfjw130_provenance a np:Provenance .
  
  dgn-np:NP892610.RA1S7R0Db_X2ubtaSzLmP2Jw3VBE63OnvyOgp13gBBfjw130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP892610.RA1S7R0Db_X2ubtaSzLmP2Jw3VBE63OnvyOgp13gBBfjw130_assertion {
  miriam-gene:5521 a ncit:C16612 .
  
  lld:C0004134 a ncit:C7057 .
  
  dgn-gda:DGNb856fd15f63a0cfe32fea2b3cfb737b4 sio:SIO_000628 miriam-gene:5521, lld:C0004134;
    a sio:SIO_001121 .
}

dgn-np:NP892610.RA1S7R0Db_X2ubtaSzLmP2Jw3VBE63OnvyOgp13gBBfjw130_provenance {
  dgn-np:NP892610.RA1S7R0Db_X2ubtaSzLmP2Jw3VBE63OnvyOgp13gBBfjw130_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-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:NP892610.RA1S7R0Db_X2ubtaSzLmP2Jw3VBE63OnvyOgp13gBBfjw130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:08+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" .
}