@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP471924.RAqwlcqCg6vdOmBsHARxjPdArHZMKO_R4_NegA6xJzyO4> .
@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:NP471924.RAqwlcqCg6vdOmBsHARxjPdArHZMKO_R4_NegA6xJzyO4130_head {
  this: np:hasAssertion dgn-np:NP471924.RAqwlcqCg6vdOmBsHARxjPdArHZMKO_R4_NegA6xJzyO4130_assertion ;
    np:hasProvenance dgn-np:NP471924.RAqwlcqCg6vdOmBsHARxjPdArHZMKO_R4_NegA6xJzyO4130_provenance ;
    np:hasPublicationInfo dgn-np:NP471924.RAqwlcqCg6vdOmBsHARxjPdArHZMKO_R4_NegA6xJzyO4130_publicationInfo ;
    a np:Nanopublication .
  dgn-np:NP471924.RAqwlcqCg6vdOmBsHARxjPdArHZMKO_R4_NegA6xJzyO4130_assertion a np:Assertion .
  dgn-np:NP471924.RAqwlcqCg6vdOmBsHARxjPdArHZMKO_R4_NegA6xJzyO4130_provenance a np:Provenance .
  dgn-np:NP471924.RAqwlcqCg6vdOmBsHARxjPdArHZMKO_R4_NegA6xJzyO4130_publicationInfo a np:PublicationInfo .
}
dgn-np:NP471924.RAqwlcqCg6vdOmBsHARxjPdArHZMKO_R4_NegA6xJzyO4130_assertion {
  miriam-gene:9001 a ncit:C16612 .
  lld:C0020179 a ncit:C7057 .
  dgn-gda:DGNb5038cde50e4d5c5e533c69e89683a55 sio:SIO_000628 miriam-gene:9001 , lld:C0020179 ;
    a sio:SIO_001121 .
}
dgn-np:NP471924.RAqwlcqCg6vdOmBsHARxjPdArHZMKO_R4_NegA6xJzyO4130_provenance {
  dgn-np:NP471924.RAqwlcqCg6vdOmBsHARxjPdArHZMKO_R4_NegA6xJzyO4130_assertion dcterms:description "[In previous candidate gene studies, associations of the age at onset (AO) in Huntington disease (HD) have been reported with genetic variations in the genes encoding adenosinergic A(2A) receptor (ADORA2A), human huntingtin-associated protein-1 (HAP1) and the single base excision repair enzyme, 7,8-dihydro-8-oxoguanine-DNA glycosylase (OGG1).]. 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:20512606 ;
    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:NP471924.RAqwlcqCg6vdOmBsHARxjPdArHZMKO_R4_NegA6xJzyO4130_publicationInfo {
  this: dcterms:created "2014-10-02T12:36:43+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" .
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}