@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ
> .
@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:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_head
{
this:
np:hasAssertion
dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_assertion
;
np:hasProvenance
dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_assertion
a
np:Assertion
.
dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_provenance
a
np:Provenance
.
dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_assertion
{
miriam-gene:6571
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN9babb723d2bdd8a8a5fa8cb6b7c48e12
sio:SIO_000628
miriam-gene:6571
,
lld:C0030567
;
a
sio:SIO_001123
.
}
dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_provenance
{
dgn-np:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_assertion
dcterms:description
"[Low expression of VMAT2 in the substantia nigra of Parkinson's disease, the involvement of VMAT2 in Lewy body of the substantia nigra suggests the association of this protein in the neurodegeneration of nigral neurons in Parkinson's disease.]. 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:16386370
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP130672.RACq_tuAf7OGGOlDj7NMNl3DRD5zej4u438a_boN1KZUQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:08+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" .
}