@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP514804.RAdZfOO1bfK7W2_r1YgDj5yDU0zDQaxpTYoH48h7pn1ow> .
@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:NP514804.RAdZfOO1bfK7W2_r1YgDj5yDU0zDQaxpTYoH48h7pn1ow130_head {
   this: np:hasAssertion dgn-np:NP514804.RAdZfOO1bfK7W2_r1YgDj5yDU0zDQaxpTYoH48h7pn1ow130_assertion ;
    np:hasProvenance dgn-np:NP514804.RAdZfOO1bfK7W2_r1YgDj5yDU0zDQaxpTYoH48h7pn1ow130_provenance ;
    np:hasPublicationInfo dgn-np:NP514804.RAdZfOO1bfK7W2_r1YgDj5yDU0zDQaxpTYoH48h7pn1ow130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP514804.RAdZfOO1bfK7W2_r1YgDj5yDU0zDQaxpTYoH48h7pn1ow130_assertion a np:Assertion .
  dgn-np:NP514804.RAdZfOO1bfK7W2_r1YgDj5yDU0zDQaxpTYoH48h7pn1ow130_provenance a np:Provenance .
  dgn-np:NP514804.RAdZfOO1bfK7W2_r1YgDj5yDU0zDQaxpTYoH48h7pn1ow130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP514804.RAdZfOO1bfK7W2_r1YgDj5yDU0zDQaxpTYoH48h7pn1ow130_assertion {
   miriam-gene:146227 a ncit:C16612 .
  lld:C0751781 a ncit:C7057 .
  dgn-gda:DGN9d6dffb5309f3e3af166cb1639e15cd5 sio:SIO_000628 miriam-gene:146227 , lld:C0751781 ;
    a sio:SIO_001121 .
}
dgn-np:NP514804.RAdZfOO1bfK7W2_r1YgDj5yDU0zDQaxpTYoH48h7pn1ow130_provenance {
   dgn-np:NP514804.RAdZfOO1bfK7W2_r1YgDj5yDU0zDQaxpTYoH48h7pn1ow130_assertion dcterms:description "[In this study we excluded SCA31 mutation from 119 unrelated patients with molecularly unassigned hereditary cerebellar ataxia, out of 512 pedigrees, after mutations in SCA1, 2, 3, 6, 7, 8, 10, 12, 17, and dentatorubral-pallidoluysian atrophy (DRPLA) had been excluded.]. 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:21163552 ;
    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:NP514804.RAdZfOO1bfK7W2_r1YgDj5yDU0zDQaxpTYoH48h7pn1ow130_publicationInfo {
   this: dcterms:created "2014-10-02T12:37:06+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" .
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}