@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP156245.RAnttkwfZagSige_W_6g0evLxjxGidN6tmsf0NjMbs6SM> .
@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:NP156245.RAnttkwfZagSige_W_6g0evLxjxGidN6tmsf0NjMbs6SM130_head {
  this: np:hasAssertion dgn-np:NP156245.RAnttkwfZagSige_W_6g0evLxjxGidN6tmsf0NjMbs6SM130_assertion ;
    np:hasProvenance dgn-np:NP156245.RAnttkwfZagSige_W_6g0evLxjxGidN6tmsf0NjMbs6SM130_provenance ;
    np:hasPublicationInfo dgn-np:NP156245.RAnttkwfZagSige_W_6g0evLxjxGidN6tmsf0NjMbs6SM130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP156245.RAnttkwfZagSige_W_6g0evLxjxGidN6tmsf0NjMbs6SM130_assertion a np:Assertion .
  dgn-np:NP156245.RAnttkwfZagSige_W_6g0evLxjxGidN6tmsf0NjMbs6SM130_provenance a np:Provenance .
  dgn-np:NP156245.RAnttkwfZagSige_W_6g0evLxjxGidN6tmsf0NjMbs6SM130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP156245.RAnttkwfZagSige_W_6g0evLxjxGidN6tmsf0NjMbs6SM130_assertion {
  miriam-gene:3064 a ncit:C16612 .
  lld:C0086132 a ncit:C7057 .
  dgn-gda:DGN656394632e4ca67608521441f16487ce sio:SIO_000628 miriam-gene:3064 , lld:C0086132 ;
    a sio:SIO_001121 .
}
dgn-np:NP156245.RAnttkwfZagSige_W_6g0evLxjxGidN6tmsf0NjMbs6SM130_provenance {
  dgn-np:NP156245.RAnttkwfZagSige_W_6g0evLxjxGidN6tmsf0NjMbs6SM130_assertion dcterms:description "[In order to examine the effects of CAG block lengths, we have correlated ApoE genotypes with the age of onset in 145 patients symptomatic for HD with psychiatric and somatic symptoms (depression, psychosis, dementia, choreic, and other movement disorders) harbouring only modestly expanded huntingtin alleles (41-45 CAGs).]. 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:15548484 ;
    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:NP156245.RAnttkwfZagSige_W_6g0evLxjxGidN6tmsf0NjMbs6SM130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:24+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" .
}