@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP425020.RAwGxPVOlAsxBwNGJ4HgBLjJxC9BYqtUGfMXTSWv3UKhE
> .
@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:NP425020.RAwGxPVOlAsxBwNGJ4HgBLjJxC9BYqtUGfMXTSWv3UKhE130_head
{
this:
np:hasAssertion
dgn-np:NP425020.RAwGxPVOlAsxBwNGJ4HgBLjJxC9BYqtUGfMXTSWv3UKhE130_assertion
;
np:hasProvenance
dgn-np:NP425020.RAwGxPVOlAsxBwNGJ4HgBLjJxC9BYqtUGfMXTSWv3UKhE130_provenance
;
np:hasPublicationInfo
dgn-np:NP425020.RAwGxPVOlAsxBwNGJ4HgBLjJxC9BYqtUGfMXTSWv3UKhE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP425020.RAwGxPVOlAsxBwNGJ4HgBLjJxC9BYqtUGfMXTSWv3UKhE130_assertion
a
np:Assertion
.
dgn-np:NP425020.RAwGxPVOlAsxBwNGJ4HgBLjJxC9BYqtUGfMXTSWv3UKhE130_provenance
a
np:Provenance
.
dgn-np:NP425020.RAwGxPVOlAsxBwNGJ4HgBLjJxC9BYqtUGfMXTSWv3UKhE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP425020.RAwGxPVOlAsxBwNGJ4HgBLjJxC9BYqtUGfMXTSWv3UKhE130_assertion
{
miriam-gene:23286
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN355ae7b5e0c232be312e2a0abc2823ec
sio:SIO_000628
miriam-gene:23286
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP425020.RAwGxPVOlAsxBwNGJ4HgBLjJxC9BYqtUGfMXTSWv3UKhE130_provenance
{
dgn-np:NP425020.RAwGxPVOlAsxBwNGJ4HgBLjJxC9BYqtUGfMXTSWv3UKhE130_assertion
dcterms:description
"[Genetic variation at the KIBRA rs17070145 polymorphism has been linked to episodic memory, executive function, and Alzheimer's disease (AD), which are related to the structural and functional integrity of the default-mode network (DMN) and executive control network (ECN).]. 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:23266749
;
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:NP425020.RAwGxPVOlAsxBwNGJ4HgBLjJxC9BYqtUGfMXTSWv3UKhE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:12+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" .
}