@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs
> .
@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 dcterms: <
http://purl.org/dc/terms/
> .
@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:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_assertion
a
np:Assertion
.
dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_provenance
a
np:Provenance
.
dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:2896
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGNd4b076921aaf665b85c5be42fc8a4cb7
sio:SIO_000628
miriam-gene:2896
,
lld:C0524851
;
a
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.
}
dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_provenance
{
dgn-np:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_assertion
dcterms:description
"[To assess the influence of rs5848 and rs646776 polymorphisms in both serum GRN level and risk for common neurodegenerative diseases, we studied 304 patients with Parkinson's disease (PD), 217 individuals with Alzheimer's disease, 131 subjects with mild cognitive impairment, and 126 controls.]. 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:23398167
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1051788.RAfVPLq8sjeYs-oAC5nvETOSZm3yHoxOgR1N1tO9BiWJs130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:43+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
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;
pav:authoredBy
<
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> , <
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> , <
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
"v4.0.0.0" .
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"v4.0.0" .
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