@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg
> .
@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:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_head
{
this:
np:hasAssertion
dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_assertion
;
np:hasProvenance
dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_provenance
;
np:hasPublicationInfo
dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_assertion
a
np:Assertion
.
dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_provenance
a
np:Provenance
.
dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_assertion
{
miriam-gene:1814
a
ncit:C16612
.
lld:C0013384
a
ncit:C7057
.
dgn-gda:DGN7bb1a3fe6a158c206f20fc42dd0699ec
sio:SIO_000628
miriam-gene:1814
,
lld:C0013384
;
a
sio:SIO_001121
.
}
dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_provenance
{
dgn-np:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_assertion
dcterms:description
"[As recent observations indicate the dopamine D(3) receptor (DRD3) to modulate both therapeutic action of levodopa and dyskinesia, we reappraised the impact of the DRD3 Ser9Gly polymorphism on development of motor complications in a large scale association study based on the gene bank of the German Competence Network on Parkinson's disease.]. 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:19353703
;
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:NP577602.RA0bY2YTkpNqm7VzH2dvXSnzw0Xm9yM6oDRMWRHkRmQxg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:48+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" .
}