@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms
> .
@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:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_head
{
this:
np:hasAssertion
dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_assertion
;
np:hasProvenance
dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_provenance
;
np:hasPublicationInfo
dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_assertion
a
np:Assertion
.
dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_provenance
a
np:Provenance
.
dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_assertion
{
miriam-gene:6531
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN806f1a8d617c73e43ee0333d6c63c813
sio:SIO_000628
miriam-gene:6531
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_provenance
{
dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_assertion
dcterms:description
"[The findings not only support an association between DAT gene and PD but also suggest the relationship of the 3'VNTR polymorphism of DAT gene with the age at the onset of 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:11774209
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
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 .
}
dgn-np:NP51554.RAbIeCJZ-LGdfvt6yd_H4So9bSFnRDnN5spZ3S_pbLNms130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}