@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP55172.RAB9IbWxzsL0-w6LaLa-Z_AE6Veq8sTku2B18bCVt0Dv0
> .
@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:NP55172.RAB9IbWxzsL0-w6LaLa-Z_AE6Veq8sTku2B18bCVt0Dv0130_head
{
this:
np:hasAssertion
dgn-np:NP55172.RAB9IbWxzsL0-w6LaLa-Z_AE6Veq8sTku2B18bCVt0Dv0130_assertion
;
np:hasProvenance
dgn-np:NP55172.RAB9IbWxzsL0-w6LaLa-Z_AE6Veq8sTku2B18bCVt0Dv0130_provenance
;
np:hasPublicationInfo
dgn-np:NP55172.RAB9IbWxzsL0-w6LaLa-Z_AE6Veq8sTku2B18bCVt0Dv0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP55172.RAB9IbWxzsL0-w6LaLa-Z_AE6Veq8sTku2B18bCVt0Dv0130_assertion
a
np:Assertion
.
dgn-np:NP55172.RAB9IbWxzsL0-w6LaLa-Z_AE6Veq8sTku2B18bCVt0Dv0130_provenance
a
np:Provenance
.
dgn-np:NP55172.RAB9IbWxzsL0-w6LaLa-Z_AE6Veq8sTku2B18bCVt0Dv0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP55172.RAB9IbWxzsL0-w6LaLa-Z_AE6Veq8sTku2B18bCVt0Dv0130_assertion
{
miriam-gene:120892
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN4b324808e46b074ec350209e3b373b67
sio:SIO_000628
miriam-gene:120892
,
lld:C0030567
;
a
sio:SIO_001122
.
}
dgn-np:NP55172.RAB9IbWxzsL0-w6LaLa-Z_AE6Veq8sTku2B18bCVt0Dv0130_provenance
{
dgn-np:NP55172.RAB9IbWxzsL0-w6LaLa-Z_AE6Veq8sTku2B18bCVt0Dv0130_assertion
dcterms:description
"[Using voxel-based morphometry in 30 asymptomatic mutation carriers (MC) with mutations in four different genes for PD and 100 healthy controls, we identified an increase in gray matter volume (GMV) in the striatum in asymptomatic Parkin, PINK1, ATP13A2 and, to a much lesser extent, in LRRK2 MC.]. 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:20483373
;
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:NP55172.RAB9IbWxzsL0-w6LaLa-Z_AE6Veq8sTku2B18bCVt0Dv0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}