@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP511280.RAjyC3F_gb1KUrxu0d-1YmfVIcigmDoQyt_qrNGuxAs5w
> .
@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:NP511280.RAjyC3F_gb1KUrxu0d-1YmfVIcigmDoQyt_qrNGuxAs5w130_head
{
this:
np:hasAssertion
dgn-np:NP511280.RAjyC3F_gb1KUrxu0d-1YmfVIcigmDoQyt_qrNGuxAs5w130_assertion
;
np:hasProvenance
dgn-np:NP511280.RAjyC3F_gb1KUrxu0d-1YmfVIcigmDoQyt_qrNGuxAs5w130_provenance
;
np:hasPublicationInfo
dgn-np:NP511280.RAjyC3F_gb1KUrxu0d-1YmfVIcigmDoQyt_qrNGuxAs5w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP511280.RAjyC3F_gb1KUrxu0d-1YmfVIcigmDoQyt_qrNGuxAs5w130_assertion
a
np:Assertion
.
dgn-np:NP511280.RAjyC3F_gb1KUrxu0d-1YmfVIcigmDoQyt_qrNGuxAs5w130_provenance
a
np:Provenance
.
dgn-np:NP511280.RAjyC3F_gb1KUrxu0d-1YmfVIcigmDoQyt_qrNGuxAs5w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP511280.RAjyC3F_gb1KUrxu0d-1YmfVIcigmDoQyt_qrNGuxAs5w130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGN485f53f2e22f5a3bde31d4f98f512cc3
sio:SIO_000628
miriam-gene:348
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP511280.RAjyC3F_gb1KUrxu0d-1YmfVIcigmDoQyt_qrNGuxAs5w130_provenance
{
dgn-np:NP511280.RAjyC3F_gb1KUrxu0d-1YmfVIcigmDoQyt_qrNGuxAs5w130_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-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:NP511280.RAjyC3F_gb1KUrxu0d-1YmfVIcigmDoQyt_qrNGuxAs5w130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:36+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}