@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP581713.RA-n_JcvC9_inqQwKQ5ul00s7jVMyH3HNJCcDU5yry1BY
> .
@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:NP581713.RA-n_JcvC9_inqQwKQ5ul00s7jVMyH3HNJCcDU5yry1BY130_head
{
this:
np:hasAssertion
dgn-np:NP581713.RA-n_JcvC9_inqQwKQ5ul00s7jVMyH3HNJCcDU5yry1BY130_assertion
;
np:hasProvenance
dgn-np:NP581713.RA-n_JcvC9_inqQwKQ5ul00s7jVMyH3HNJCcDU5yry1BY130_provenance
;
np:hasPublicationInfo
dgn-np:NP581713.RA-n_JcvC9_inqQwKQ5ul00s7jVMyH3HNJCcDU5yry1BY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP581713.RA-n_JcvC9_inqQwKQ5ul00s7jVMyH3HNJCcDU5yry1BY130_assertion
a
np:Assertion
.
dgn-np:NP581713.RA-n_JcvC9_inqQwKQ5ul00s7jVMyH3HNJCcDU5yry1BY130_provenance
a
np:Provenance
.
dgn-np:NP581713.RA-n_JcvC9_inqQwKQ5ul00s7jVMyH3HNJCcDU5yry1BY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP581713.RA-n_JcvC9_inqQwKQ5ul00s7jVMyH3HNJCcDU5yry1BY130_assertion
{
miriam-gene:2048
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNf6e0f6588d58c70ac74d8d076538835e
sio:SIO_000628
miriam-gene:2048
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP581713.RA-n_JcvC9_inqQwKQ5ul00s7jVMyH3HNJCcDU5yry1BY130_provenance
{
dgn-np:NP581713.RA-n_JcvC9_inqQwKQ5ul00s7jVMyH3HNJCcDU5yry1BY130_assertion
dcterms:description
"[We aimed to assess whether allelic variants of dopamine receptor, glutamate receptor, and serotonin transporter genes are associated with the appearance of impulse control and related behaviors (ICRB) in Parkinson's disease (PD) with dopamine replacement therapy (DRT).]. 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:19562769
;
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:NP581713.RA-n_JcvC9_inqQwKQ5ul00s7jVMyH3HNJCcDU5yry1BY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:50+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" .
}