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http://rdf.disgenet.org/nanopublications.trig#NP867367.RATJ53r2uCy1-6IYENcO_X37WXkjj_PSBpS649lKT8xak
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP867367.RATJ53r2uCy1-6IYENcO_X37WXkjj_PSBpS649lKT8xak130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
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dgn-np:NP867367.RATJ53r2uCy1-6IYENcO_X37WXkjj_PSBpS649lKT8xak130_assertion
a
np:Assertion
.
dgn-np:NP867367.RATJ53r2uCy1-6IYENcO_X37WXkjj_PSBpS649lKT8xak130_provenance
a
np:Provenance
.
dgn-np:NP867367.RATJ53r2uCy1-6IYENcO_X37WXkjj_PSBpS649lKT8xak130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:1861
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN8906f3709516876dfca690436841455d
sio:SIO_000628
miriam-gene:1861
,
lld:C0030567
;
a
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.
}
dgn-np:NP867367.RATJ53r2uCy1-6IYENcO_X37WXkjj_PSBpS649lKT8xak130_provenance
{
dgn-np:NP867367.RATJ53r2uCy1-6IYENcO_X37WXkjj_PSBpS649lKT8xak130_assertion
dcterms:description
"[Moreover, dystonia and Parkinson disease share the common feature of reduced dopamine neurotransmission in the striatum, so we assumed that mutations in the DYT1 gene might have the same role in cases of early onset primary torsion dystonia (EOPTD) and early onset Parkinson disease (EOPD) that present 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:19038309
;
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:NP867367.RATJ53r2uCy1-6IYENcO_X37WXkjj_PSBpS649lKT8xak130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:50+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
<
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> , <
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> , <
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
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