@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_head
{
this:
np:hasAssertion
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_assertion
;
np:hasProvenance
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_provenance
;
np:hasPublicationInfo
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_assertion
a
np:Assertion
.
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_provenance
a
np:Provenance
.
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_assertion
{
miriam-gene:5071
a
ncit:C16612
.
lld:C3160718
a
ncit:C7057
.
dgn-gda:DGN67182c755ac8dc348f20e6ed279487bf
sio:SIO_000628
miriam-gene:5071
,
lld:C3160718
;
a
sio:SIO_001122
.
}
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_provenance
{
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_assertion
dcterms:description
"[A wide variety of mutations in the parkin gene are responsible for autosomal recessive parkinsonism in Europe. French Parkinson's Disease Genetics Study Group and the European Consortium on Genetic Susceptibility 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_curated
;
sio:SIO_000772
miriam-pubmed:10072423
;
prov:wasDerivedFrom
dgn-void:uniprot-2016
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
dgn-void:uniprot-2016
pav:importedOn
"2016-01-25"^^
xsd:date
.
}
dgn-np:NP36.RArBbFbaETF1r94SEwkLNHJG7kNudLtSZgNSuCFetbJaY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:41:50+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:disgenetv3.0rdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}