@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP89051.RAUKMZVaeiRzcz-W9kKS8IglJZImbddL0RmpfaBpVxTIY
> .
@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:NP89051.RAUKMZVaeiRzcz-W9kKS8IglJZImbddL0RmpfaBpVxTIY130_head
{
this:
np:hasAssertion
dgn-np:NP89051.RAUKMZVaeiRzcz-W9kKS8IglJZImbddL0RmpfaBpVxTIY130_assertion
;
np:hasProvenance
dgn-np:NP89051.RAUKMZVaeiRzcz-W9kKS8IglJZImbddL0RmpfaBpVxTIY130_provenance
;
np:hasPublicationInfo
dgn-np:NP89051.RAUKMZVaeiRzcz-W9kKS8IglJZImbddL0RmpfaBpVxTIY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP89051.RAUKMZVaeiRzcz-W9kKS8IglJZImbddL0RmpfaBpVxTIY130_assertion
a
np:Assertion
.
dgn-np:NP89051.RAUKMZVaeiRzcz-W9kKS8IglJZImbddL0RmpfaBpVxTIY130_provenance
a
np:Provenance
.
dgn-np:NP89051.RAUKMZVaeiRzcz-W9kKS8IglJZImbddL0RmpfaBpVxTIY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP89051.RAUKMZVaeiRzcz-W9kKS8IglJZImbddL0RmpfaBpVxTIY130_assertion
{
miriam-gene:1471
a
ncit:C16612
.
lld:C0497327
a
ncit:C7057
.
dgn-gda:DGN9515b358295530502e292c3b2a15527e
sio:SIO_000628
miriam-gene:1471
,
lld:C0497327
;
a
sio:SIO_001122
.
}
dgn-np:NP89051.RAUKMZVaeiRzcz-W9kKS8IglJZImbddL0RmpfaBpVxTIY130_provenance
{
dgn-np:NP89051.RAUKMZVaeiRzcz-W9kKS8IglJZImbddL0RmpfaBpVxTIY130_assertion
dcterms:description
"[The CST3 BB genotype leads to a reduced secretion of the protein in vitro and increases the risk for AD, suggesting that variability in the CST3 gene and CysC protein concentration may be associated with dementia in Lewy body 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:20157249
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP89051.RAUKMZVaeiRzcz-W9kKS8IglJZImbddL0RmpfaBpVxTIY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:44+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" .
}