@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP192751.RAKMdb0482VYRKnLM8Lau6tCvhpPIIuYot6eu6cJUjBBw
> .
@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:NP192751.RAKMdb0482VYRKnLM8Lau6tCvhpPIIuYot6eu6cJUjBBw130_head
{
this:
np:hasAssertion
dgn-np:NP192751.RAKMdb0482VYRKnLM8Lau6tCvhpPIIuYot6eu6cJUjBBw130_assertion
;
np:hasProvenance
dgn-np:NP192751.RAKMdb0482VYRKnLM8Lau6tCvhpPIIuYot6eu6cJUjBBw130_provenance
;
np:hasPublicationInfo
dgn-np:NP192751.RAKMdb0482VYRKnLM8Lau6tCvhpPIIuYot6eu6cJUjBBw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP192751.RAKMdb0482VYRKnLM8Lau6tCvhpPIIuYot6eu6cJUjBBw130_assertion
a
np:Assertion
.
dgn-np:NP192751.RAKMdb0482VYRKnLM8Lau6tCvhpPIIuYot6eu6cJUjBBw130_provenance
a
np:Provenance
.
dgn-np:NP192751.RAKMdb0482VYRKnLM8Lau6tCvhpPIIuYot6eu6cJUjBBw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP192751.RAKMdb0482VYRKnLM8Lau6tCvhpPIIuYot6eu6cJUjBBw130_assertion
{
miriam-gene:1861
a
ncit:C16612
.
lld:C0013421
a
ncit:C7057
.
dgn-gda:DGNe60818c91945bc9bca22aa29c05310f6
sio:SIO_000628
miriam-gene:1861
,
lld:C0013421
;
a
sio:SIO_001121
.
}
dgn-np:NP192751.RAKMdb0482VYRKnLM8Lau6tCvhpPIIuYot6eu6cJUjBBw130_provenance
{
dgn-np:NP192751.RAKMdb0482VYRKnLM8Lau6tCvhpPIIuYot6eu6cJUjBBw130_assertion
dcterms:description
"[Our findings collectively suggest that altered communication between cholinergic interneurons and medium spiny neurons is responsible for the LTD deficit and that this synaptic plasticity modification may be involved in the striatal motor control abnormalities in our mouse model of DYT1 dystonia.]. 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:21995941
;
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 .
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dgn-np:NP192751.RAKMdb0482VYRKnLM8Lau6tCvhpPIIuYot6eu6cJUjBBw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:46+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" .
}