@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP547557.RATSQoxHuwFNISHLAOlte1YnGRdisOXCqks4wWS7coXgQ
> .
@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:NP547557.RATSQoxHuwFNISHLAOlte1YnGRdisOXCqks4wWS7coXgQ130_head
{
this:
np:hasAssertion
dgn-np:NP547557.RATSQoxHuwFNISHLAOlte1YnGRdisOXCqks4wWS7coXgQ130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP547557.RATSQoxHuwFNISHLAOlte1YnGRdisOXCqks4wWS7coXgQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP547557.RATSQoxHuwFNISHLAOlte1YnGRdisOXCqks4wWS7coXgQ130_assertion
a
np:Assertion
.
dgn-np:NP547557.RATSQoxHuwFNISHLAOlte1YnGRdisOXCqks4wWS7coXgQ130_provenance
a
np:Provenance
.
dgn-np:NP547557.RATSQoxHuwFNISHLAOlte1YnGRdisOXCqks4wWS7coXgQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP547557.RATSQoxHuwFNISHLAOlte1YnGRdisOXCqks4wWS7coXgQ130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0085923
a
ncit:C7057
.
dgn-gda:DGN5b834a3556fae11036b71cd1b54ff9c9
sio:SIO_000628
miriam-gene:348
,
lld:C0085923
;
a
sio:SIO_001121
.
}
dgn-np:NP547557.RATSQoxHuwFNISHLAOlte1YnGRdisOXCqks4wWS7coXgQ130_provenance
{
dgn-np:NP547557.RATSQoxHuwFNISHLAOlte1YnGRdisOXCqks4wWS7coXgQ130_assertion
dcterms:description
"[The association with age and the APOE epsilon4 genotype suggests that the systematic investigation of NSS may contribute to identify subjects at risk of clinically significant cognitive decline in later life.]. 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:16131735
;
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:NP547557.RATSQoxHuwFNISHLAOlte1YnGRdisOXCqks4wWS7coXgQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:30+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" .
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"v2.1.0" .
}