@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP484265.RADHmlyomBJFXdHo4mfyfCerw0X7YjKoH5fnobEZUvmkk
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
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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#
> .
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{
this:
np:hasAssertion
dgn-np:NP484265.RADHmlyomBJFXdHo4mfyfCerw0X7YjKoH5fnobEZUvmkk130_assertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP484265.RADHmlyomBJFXdHo4mfyfCerw0X7YjKoH5fnobEZUvmkk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP484265.RADHmlyomBJFXdHo4mfyfCerw0X7YjKoH5fnobEZUvmkk130_assertion
a
np:Assertion
.
dgn-np:NP484265.RADHmlyomBJFXdHo4mfyfCerw0X7YjKoH5fnobEZUvmkk130_provenance
a
np:Provenance
.
dgn-np:NP484265.RADHmlyomBJFXdHo4mfyfCerw0X7YjKoH5fnobEZUvmkk130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP484265.RADHmlyomBJFXdHo4mfyfCerw0X7YjKoH5fnobEZUvmkk130_assertion
{
miriam-gene:255239
a
ncit:C16612
.
lld:C0013384
a
ncit:C7057
.
dgn-gda:DGNec0c33aa6be599868de7bcdfc23ebe17
sio:SIO_000628
miriam-gene:255239
,
lld:C0013384
;
a
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.
}
dgn-np:NP484265.RADHmlyomBJFXdHo4mfyfCerw0X7YjKoH5fnobEZUvmkk130_provenance
{
dgn-np:NP484265.RADHmlyomBJFXdHo4mfyfCerw0X7YjKoH5fnobEZUvmkk130_assertion
dcterms:description
"[Since genetic factors could play a role in determining the occurrence of these problems, the aim of the present study was to investigate whether possible functional polymorphisms among DRD2 and ANKK1 genes are associated with the risk of developing dyskinesia and motor fluctuations in Parkinson's disease patients.]. 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:23171335
;
prov:wasDerivedFrom
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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 .
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dgn-np:NP484265.RADHmlyomBJFXdHo4mfyfCerw0X7YjKoH5fnobEZUvmkk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:49+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
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> , <
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> , <
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http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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