@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" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}