@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY> .
@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:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_head {
  this: np:hasAssertion dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_assertion;
    np:hasProvenance dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_provenance;
    np:hasPublicationInfo dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_assertion a np:Assertion .
  
  dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_provenance a np:Provenance .
  
  dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_assertion {
  miriam-gene:3064 a ncit:C16612 .
  
  lld:C0087012 a ncit:C7057 .
  
  dgn-gda:DGN125a609714ba7330397b964483d416a7 sio:SIO_000628 miriam-gene:3064, lld:C0087012;
    a sio:SIO_001121 .
}

dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_provenance {
  dgn-np:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_assertion dcterms:description
      "[The two shorter constructs containing the beta A4 sequence formed similar intranuclear aggregates to those reported for intranuclear inclusions of polyglutamine peptides from huntingtin (in Huntington's disease) and ataxin protein fragments (in spinocerebellar 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:9686302;
    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:NP649342.RANGYTX_nED8GeT8sh4HeYnP5C1X8LW3mRPOj1K-xOvKY130_publicationInfo {
  this: dcterms:created "2014-10-02T12:38:31+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" .
}