@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP925268.RAY2-tooPCvS5Fy89rdFbgChro2cKLSNTz6uMkXD6yPPg> .
@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:NP925268.RAY2-tooPCvS5Fy89rdFbgChro2cKLSNTz6uMkXD6yPPg130_head {
  this: np:hasAssertion dgn-np:NP925268.RAY2-tooPCvS5Fy89rdFbgChro2cKLSNTz6uMkXD6yPPg130_assertion;
    np:hasProvenance dgn-np:NP925268.RAY2-tooPCvS5Fy89rdFbgChro2cKLSNTz6uMkXD6yPPg130_provenance;
    np:hasPublicationInfo dgn-np:NP925268.RAY2-tooPCvS5Fy89rdFbgChro2cKLSNTz6uMkXD6yPPg130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP925268.RAY2-tooPCvS5Fy89rdFbgChro2cKLSNTz6uMkXD6yPPg130_assertion a np:Assertion .
  
  dgn-np:NP925268.RAY2-tooPCvS5Fy89rdFbgChro2cKLSNTz6uMkXD6yPPg130_provenance a np:Provenance .
  
  dgn-np:NP925268.RAY2-tooPCvS5Fy89rdFbgChro2cKLSNTz6uMkXD6yPPg130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP925268.RAY2-tooPCvS5Fy89rdFbgChro2cKLSNTz6uMkXD6yPPg130_assertion {
  miriam-gene:1822 a ncit:C16612 .
  
  lld:C0007758 a ncit:C7057 .
  
  dgn-gda:DGN8d16b1869c9e7e73fab0c4001882e533 sio:SIO_000628 miriam-gene:1822, lld:C0007758;
    a sio:SIO_001121 .
}

dgn-np:NP925268.RAY2-tooPCvS5Fy89rdFbgChro2cKLSNTz6uMkXD6yPPg130_provenance {
  dgn-np:NP925268.RAY2-tooPCvS5Fy89rdFbgChro2cKLSNTz6uMkXD6yPPg130_assertion dcterms:description
      "[In addition, because of the clinical overlap between patients with HDL disease and autosomal dominant cerebellar ataxia or dentatorubral and pallidoluysian atrophy (DRPLA), we investigated trinucleotide repeat expansions in genes encoding the TATA-binding protein (TBP/SCA17) and atrophin-1 (DRPLA).]. 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:12805114;
    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:NP925268.RAY2-tooPCvS5Fy89rdFbgChro2cKLSNTz6uMkXD6yPPg130_publicationInfo {
  this: dcterms:created "2014-10-02T12:41:27+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" .
}