@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc
> .
@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:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_head
{
this:
np:hasAssertion
dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_assertion
;
np:hasProvenance
dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_provenance
;
np:hasPublicationInfo
dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_assertion
a
np:Assertion
.
dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_provenance
a
np:Provenance
.
dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_assertion
{
miriam-gene:1814
a
ncit:C16612
.
lld:C0270736
a
ncit:C7057
.
dgn-gda:DGNce535f83ad60960e08877f5a74507c76
sio:SIO_000628
miriam-gene:1814
,
lld:C0270736
;
a
sio:SIO_001121
.
}
dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_provenance
{
dgn-np:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_assertion
dcterms:description
"[These results suggest that DRD3 genotype and the variant DRD3Gly allelic variant is associated with the risk for and age at onset of ET, and with the risk for voice tremor, in Caucasian Spanish people.]. 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:19645064
;
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:NP279811.RADiSZfO6c-uh3DLBTnW-0rM-XHpfjWRtZ7-wh0kjjvqc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}