@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP489043.RA3rifEOhBB9jJSqFeH__ujtUWpFCFM797fO3JXoFrwAE
> .
@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:NP489043.RA3rifEOhBB9jJSqFeH__ujtUWpFCFM797fO3JXoFrwAE130_head
{
this:
np:hasAssertion
dgn-np:NP489043.RA3rifEOhBB9jJSqFeH__ujtUWpFCFM797fO3JXoFrwAE130_assertion
;
np:hasProvenance
dgn-np:NP489043.RA3rifEOhBB9jJSqFeH__ujtUWpFCFM797fO3JXoFrwAE130_provenance
;
np:hasPublicationInfo
dgn-np:NP489043.RA3rifEOhBB9jJSqFeH__ujtUWpFCFM797fO3JXoFrwAE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP489043.RA3rifEOhBB9jJSqFeH__ujtUWpFCFM797fO3JXoFrwAE130_assertion
a
np:Assertion
.
dgn-np:NP489043.RA3rifEOhBB9jJSqFeH__ujtUWpFCFM797fO3JXoFrwAE130_provenance
a
np:Provenance
.
dgn-np:NP489043.RA3rifEOhBB9jJSqFeH__ujtUWpFCFM797fO3JXoFrwAE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP489043.RA3rifEOhBB9jJSqFeH__ujtUWpFCFM797fO3JXoFrwAE130_assertion
{
miriam-gene:470
a
ncit:C16612
.
lld:C0030567
a
ncit:C7057
.
dgn-gda:DGN72b784a9be91b53385ae45fa2a90d82f
sio:SIO_000628
miriam-gene:470
,
lld:C0030567
;
a
sio:SIO_001121
.
}
dgn-np:NP489043.RA3rifEOhBB9jJSqFeH__ujtUWpFCFM797fO3JXoFrwAE130_provenance
{
dgn-np:NP489043.RA3rifEOhBB9jJSqFeH__ujtUWpFCFM797fO3JXoFrwAE130_assertion
dcterms:description
"[The fact that mutant alpha-synucleins inhibit ALP functioning by tightly binding to the receptor on the lysosomal membrane for autophagy pathway further supports the assumption that impairment of the ALP may be related to the development of 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:18187492
;
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:NP489043.RA3rifEOhBB9jJSqFeH__ujtUWpFCFM797fO3JXoFrwAE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:52+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" .
}