@prefix this: <http://rdf.disgenet.org/resource/nanopub/NP1345612.RAnuHAVPaGWRGGheL3uGk_LpTAUjneWpr59cFU5T25XFg> .
@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:NP1345612.RAnuHAVPaGWRGGheL3uGk_LpTAUjneWpr59cFU5T25XFg130_head {
  this: np:hasAssertion dgn-np:NP1345612.RAnuHAVPaGWRGGheL3uGk_LpTAUjneWpr59cFU5T25XFg130_assertion;
    np:hasProvenance dgn-np:NP1345612.RAnuHAVPaGWRGGheL3uGk_LpTAUjneWpr59cFU5T25XFg130_provenance;
    np:hasPublicationInfo dgn-np:NP1345612.RAnuHAVPaGWRGGheL3uGk_LpTAUjneWpr59cFU5T25XFg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP1345612.RAnuHAVPaGWRGGheL3uGk_LpTAUjneWpr59cFU5T25XFg130_assertion a np:Assertion .
  
  dgn-np:NP1345612.RAnuHAVPaGWRGGheL3uGk_LpTAUjneWpr59cFU5T25XFg130_provenance a np:Provenance .
  
  dgn-np:NP1345612.RAnuHAVPaGWRGGheL3uGk_LpTAUjneWpr59cFU5T25XFg130_publicationInfo
    a np:PublicationInfo .
}

dgn-np:NP1345612.RAnuHAVPaGWRGGheL3uGk_LpTAUjneWpr59cFU5T25XFg130_assertion {
  miriam-gene:6310 a ncit:C16612 .
  
  lld:C0024408 a ncit:C7057 .
  
  dgn-gda:DGNb08529297811302e5b58ef5a62b30743 sio:SIO_000628 miriam-gene:6310, lld:C0024408;
    a sio:SIO_001121 .
}

dgn-np:NP1345612.RAnuHAVPaGWRGGheL3uGk_LpTAUjneWpr59cFU5T25XFg130_provenance {
  dgn-np:NP1345612.RAnuHAVPaGWRGGheL3uGk_LpTAUjneWpr59cFU5T25XFg130_assertion dcterms:description
      "[These results suggest that SCA may be occasionally caused by the SCA1 mutation and rarely caused by the DRPLA mutation and that, to date, the MJD mutation seems to be the most common cause of dominantly inherited SCA.]. 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:8559378;
    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:NP1345612.RAnuHAVPaGWRGGheL3uGk_LpTAUjneWpr59cFU5T25XFg130_publicationInfo {
  this: dcterms:created "2016-05-13T12:51:56+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" .
}