@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP431021.RABbWWbd03Ut4XLA7q9n9NWijvOSrrox8DtM92lTUW_Yw
> .
@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:NP431021.RABbWWbd03Ut4XLA7q9n9NWijvOSrrox8DtM92lTUW_Yw130_assertion
;
np:hasProvenance
dgn-np:NP431021.RABbWWbd03Ut4XLA7q9n9NWijvOSrrox8DtM92lTUW_Yw130_provenance
;
np:hasPublicationInfo
dgn-np:NP431021.RABbWWbd03Ut4XLA7q9n9NWijvOSrrox8DtM92lTUW_Yw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP431021.RABbWWbd03Ut4XLA7q9n9NWijvOSrrox8DtM92lTUW_Yw130_assertion
a
np:Assertion
.
dgn-np:NP431021.RABbWWbd03Ut4XLA7q9n9NWijvOSrrox8DtM92lTUW_Yw130_provenance
a
np:Provenance
.
dgn-np:NP431021.RABbWWbd03Ut4XLA7q9n9NWijvOSrrox8DtM92lTUW_Yw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP431021.RABbWWbd03Ut4XLA7q9n9NWijvOSrrox8DtM92lTUW_Yw130_assertion
{
miriam-gene:2019
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGNd071d03f6621f128016f6cefa6f23bf2
sio:SIO_000628
miriam-gene:2019
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP431021.RABbWWbd03Ut4XLA7q9n9NWijvOSrrox8DtM92lTUW_Yw130_provenance
{
dgn-np:NP431021.RABbWWbd03Ut4XLA7q9n9NWijvOSrrox8DtM92lTUW_Yw130_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 ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:19345444
;
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:NP431021.RABbWWbd03Ut4XLA7q9n9NWijvOSrrox8DtM92lTUW_Yw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}