@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP782494.RAI3Dj4vsWFzdGyUHuCAUvOsfdVDR8d7NZr3JHK7eNoOI> .
@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:NP782494.RAI3Dj4vsWFzdGyUHuCAUvOsfdVDR8d7NZr3JHK7eNoOI130_head {
  this: np:hasAssertion dgn-np:NP782494.RAI3Dj4vsWFzdGyUHuCAUvOsfdVDR8d7NZr3JHK7eNoOI130_assertion ;
    np:hasProvenance dgn-np:NP782494.RAI3Dj4vsWFzdGyUHuCAUvOsfdVDR8d7NZr3JHK7eNoOI130_provenance ;
    np:hasPublicationInfo dgn-np:NP782494.RAI3Dj4vsWFzdGyUHuCAUvOsfdVDR8d7NZr3JHK7eNoOI130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP782494.RAI3Dj4vsWFzdGyUHuCAUvOsfdVDR8d7NZr3JHK7eNoOI130_assertion a np:Assertion .
  dgn-np:NP782494.RAI3Dj4vsWFzdGyUHuCAUvOsfdVDR8d7NZr3JHK7eNoOI130_provenance a np:Provenance .
  dgn-np:NP782494.RAI3Dj4vsWFzdGyUHuCAUvOsfdVDR8d7NZr3JHK7eNoOI130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP782494.RAI3Dj4vsWFzdGyUHuCAUvOsfdVDR8d7NZr3JHK7eNoOI130_assertion {
  miriam-gene:3918 a ncit:C16612 .
  lld:C0020179 a ncit:C7057 .
  dgn-gda:DGN5eb88eb08346a5caf5f8b61fcfa5a805 sio:SIO_000628 miriam-gene:3918 , lld:C0020179 ;
    a sio:SIO_001121 .
}
dgn-np:NP782494.RAI3Dj4vsWFzdGyUHuCAUvOsfdVDR8d7NZr3JHK7eNoOI130_provenance {
  dgn-np:NP782494.RAI3Dj4vsWFzdGyUHuCAUvOsfdVDR8d7NZr3JHK7eNoOI130_assertion dcterms:description "[We report a non-familial Huntington's disease (HD) patient presenting with increased levels of protein and IgG in his cerebrospinal fluid (CSF), antineuronal antibody in his serum and CSF, Purkinje cell and granule cell degeneration in the cerebellum, and grumose degeneration in the dentate nucleus, in addition to typical HD findings.]. 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:10348164 ;
    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:NP782494.RAI3Dj4vsWFzdGyUHuCAUvOsfdVDR8d7NZr3JHK7eNoOI130_publicationInfo {
  this: dcterms:created "2014-10-02T12:39:54+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" .
}