@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP68263.RAnBeKJ4hSP9joYkmt3D5oc3KNiHDm-xTCuABPTrilk2c
> .
@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:
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP68263.RAnBeKJ4hSP9joYkmt3D5oc3KNiHDm-xTCuABPTrilk2c130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP68263.RAnBeKJ4hSP9joYkmt3D5oc3KNiHDm-xTCuABPTrilk2c130_provenance
a
np:Provenance
.
dgn-np:NP68263.RAnBeKJ4hSP9joYkmt3D5oc3KNiHDm-xTCuABPTrilk2c130_publicationInfo
a
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.
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{
miriam-gene:5309
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNc5ad4c3a6974caf48b5e1a4d10c6dcd8
sio:SIO_000628
miriam-gene:5309
,
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.
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dgn-np:NP68263.RAnBeKJ4hSP9joYkmt3D5oc3KNiHDm-xTCuABPTrilk2c130_provenance
{
dgn-np:NP68263.RAnBeKJ4hSP9joYkmt3D5oc3KNiHDm-xTCuABPTrilk2c130_assertion
dcterms:description
"[In particular, our highly significant findings regarding the association of rs3758549 reproduce the results of the initial report on transcription factor gene variants, providing further evidence for PITX3 and EN1 polymorphisms as potential genetic risk factors for sporadic PD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:19345444
;
prov:wasDerivedFrom
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;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP68263.RAnBeKJ4hSP9joYkmt3D5oc3KNiHDm-xTCuABPTrilk2c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:32+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
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prv:usedData
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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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