@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y
> .
@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:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_head
{
this:
np:hasAssertion
dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_assertion
;
np:hasProvenance
dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_assertion
a
np:Assertion
.
dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_provenance
a
np:Provenance
.
dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_assertion
{
miriam-gene:120892
a
ncit:C16612
.
lld:C0752347
a
ncit:C7057
.
dgn-gda:DGN3873f35e863f3ff5dddab696f761756a
sio:SIO_000628
miriam-gene:120892
,
lld:C0752347
;
a
sio:SIO_001121
.
}
dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_provenance
{
dgn-np:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_assertion
dcterms:description
"[Neuropathology is characterized by loss of dopaminergic neurons in the substantia nigra pars compacta in all cases with accompanying Lewy pathology, or tau pathology or without intraneuronal inclusions, thus indicating that mutations in LRRK2 are not always manifested as Lewy body disease (LBD) or as alpha-synucleinopathy.]. 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:19142648
;
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:NP251384.RAbR0NNCoJlUf3mc-baVBSzla2AcyK9wEoSMlwYS_CC0Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}