@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP609508.RAB0OlQGvpcj4ZfkzNyL7i936aQkvtgjOMJC9R9LbEXYk
> .
@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:NP609508.RAB0OlQGvpcj4ZfkzNyL7i936aQkvtgjOMJC9R9LbEXYk130_head
{
this:
np:hasAssertion
dgn-np:NP609508.RAB0OlQGvpcj4ZfkzNyL7i936aQkvtgjOMJC9R9LbEXYk130_assertion
;
np:hasProvenance
dgn-np:NP609508.RAB0OlQGvpcj4ZfkzNyL7i936aQkvtgjOMJC9R9LbEXYk130_provenance
;
np:hasPublicationInfo
dgn-np:NP609508.RAB0OlQGvpcj4ZfkzNyL7i936aQkvtgjOMJC9R9LbEXYk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP609508.RAB0OlQGvpcj4ZfkzNyL7i936aQkvtgjOMJC9R9LbEXYk130_assertion
a
np:Assertion
.
dgn-np:NP609508.RAB0OlQGvpcj4ZfkzNyL7i936aQkvtgjOMJC9R9LbEXYk130_provenance
a
np:Provenance
.
dgn-np:NP609508.RAB0OlQGvpcj4ZfkzNyL7i936aQkvtgjOMJC9R9LbEXYk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP609508.RAB0OlQGvpcj4ZfkzNyL7i936aQkvtgjOMJC9R9LbEXYk130_assertion
{
miriam-gene:1812
a
ncit:C16612
.
lld:C0030662
a
ncit:C7057
.
dgn-gda:DGNe3ec4d6dd2957b7fcf3962bf15bf93d2
sio:SIO_000628
miriam-gene:1812
,
lld:C0030662
;
a
sio:SIO_001121
.
}
dgn-np:NP609508.RAB0OlQGvpcj4ZfkzNyL7i936aQkvtgjOMJC9R9LbEXYk130_provenance
{
dgn-np:NP609508.RAB0OlQGvpcj4ZfkzNyL7i936aQkvtgjOMJC9R9LbEXYk130_assertion
dcterms:description
"[The present study aimed to investigate whether selected polymorphisms in the dopamine receptors genes (DRD1, DRD2, DRD3, and DRD4) are associated with PG in Korean population which is consisted of only Korean ancestry.]. 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:21853233
;
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:NP609508.RAB0OlQGvpcj4ZfkzNyL7i936aQkvtgjOMJC9R9LbEXYk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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" .
}