@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP660646.RANBQNiHWzWSP9PEdeYGcDwfG712735UAnKzWAxL93k0M
> .
@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:NP660646.RANBQNiHWzWSP9PEdeYGcDwfG712735UAnKzWAxL93k0M130_head
{
this:
np:hasAssertion
dgn-np:NP660646.RANBQNiHWzWSP9PEdeYGcDwfG712735UAnKzWAxL93k0M130_assertion
;
np:hasProvenance
dgn-np:NP660646.RANBQNiHWzWSP9PEdeYGcDwfG712735UAnKzWAxL93k0M130_provenance
;
np:hasPublicationInfo
dgn-np:NP660646.RANBQNiHWzWSP9PEdeYGcDwfG712735UAnKzWAxL93k0M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP660646.RANBQNiHWzWSP9PEdeYGcDwfG712735UAnKzWAxL93k0M130_assertion
a
np:Assertion
.
dgn-np:NP660646.RANBQNiHWzWSP9PEdeYGcDwfG712735UAnKzWAxL93k0M130_provenance
a
np:Provenance
.
dgn-np:NP660646.RANBQNiHWzWSP9PEdeYGcDwfG712735UAnKzWAxL93k0M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP660646.RANBQNiHWzWSP9PEdeYGcDwfG712735UAnKzWAxL93k0M130_assertion
{
miriam-gene:1813
a
ncit:C16612
.
lld:C0030662
a
ncit:C7057
.
dgn-gda:DGN75aa84fed12f8f5ffa354c589e6b39e9
sio:SIO_000628
miriam-gene:1813
,
lld:C0030662
;
a
sio:SIO_001121
.
}
dgn-np:NP660646.RANBQNiHWzWSP9PEdeYGcDwfG712735UAnKzWAxL93k0M130_provenance
{
dgn-np:NP660646.RANBQNiHWzWSP9PEdeYGcDwfG712735UAnKzWAxL93k0M130_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:NP660646.RANBQNiHWzWSP9PEdeYGcDwfG712735UAnKzWAxL93k0M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:39+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" .
}