@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP556176.RAPyzF_0RKET0yFiji-MkX75MP1uHITuzTjGbq5Eirm2w> .
@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:NP556176.RAPyzF_0RKET0yFiji-MkX75MP1uHITuzTjGbq5Eirm2w130_head {
  this: np:hasAssertion dgn-np:NP556176.RAPyzF_0RKET0yFiji-MkX75MP1uHITuzTjGbq5Eirm2w130_assertion;
    np:hasProvenance dgn-np:NP556176.RAPyzF_0RKET0yFiji-MkX75MP1uHITuzTjGbq5Eirm2w130_provenance;
    np:hasPublicationInfo dgn-np:NP556176.RAPyzF_0RKET0yFiji-MkX75MP1uHITuzTjGbq5Eirm2w130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP556176.RAPyzF_0RKET0yFiji-MkX75MP1uHITuzTjGbq5Eirm2w130_assertion a np:Assertion .
  
  dgn-np:NP556176.RAPyzF_0RKET0yFiji-MkX75MP1uHITuzTjGbq5Eirm2w130_provenance a np:Provenance .
  
  dgn-np:NP556176.RAPyzF_0RKET0yFiji-MkX75MP1uHITuzTjGbq5Eirm2w130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP556176.RAPyzF_0RKET0yFiji-MkX75MP1uHITuzTjGbq5Eirm2w130_assertion {
  miriam-gene:2395 a ncit:C16612 .
  
  lld:C0393524 a ncit:C7057 .
  
  dgn-gda:DGN1e8896d940d052ae0372c39402f2b570 sio:SIO_000628 miriam-gene:2395, lld:C0393524;
    a sio:SIO_001121 .
}

dgn-np:NP556176.RAPyzF_0RKET0yFiji-MkX75MP1uHITuzTjGbq5Eirm2w130_provenance {
  dgn-np:NP556176.RAPyzF_0RKET0yFiji-MkX75MP1uHITuzTjGbq5Eirm2w130_assertion dcterms:description
      "[We identified 76 index cases of LOCA, of whom 63 were sporadic, idiopathic LOCA (ILOCA) and 13 were familial LOCA, of whom six had either spinocerebellar ataxia type 6, Friedreich's ataxia or dominant episodic ataxia.]. 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:15258214;
    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:NP556176.RAPyzF_0RKET0yFiji-MkX75MP1uHITuzTjGbq5Eirm2w130_publicationInfo {
  this: dcterms:created "2014-10-02T12:37:35+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" .
}