@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP499465.RATT3gaa2E37-9Dxq778dHSJKL_oEWgT5UgLa3rtITh_0
> .
@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:NP499465.RATT3gaa2E37-9Dxq778dHSJKL_oEWgT5UgLa3rtITh_0130_head
{
this:
np:hasAssertion
dgn-np:NP499465.RATT3gaa2E37-9Dxq778dHSJKL_oEWgT5UgLa3rtITh_0130_assertion
;
np:hasProvenance
dgn-np:NP499465.RATT3gaa2E37-9Dxq778dHSJKL_oEWgT5UgLa3rtITh_0130_provenance
;
np:hasPublicationInfo
dgn-np:NP499465.RATT3gaa2E37-9Dxq778dHSJKL_oEWgT5UgLa3rtITh_0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP499465.RATT3gaa2E37-9Dxq778dHSJKL_oEWgT5UgLa3rtITh_0130_assertion
a
np:Assertion
.
dgn-np:NP499465.RATT3gaa2E37-9Dxq778dHSJKL_oEWgT5UgLa3rtITh_0130_provenance
a
np:Provenance
.
dgn-np:NP499465.RATT3gaa2E37-9Dxq778dHSJKL_oEWgT5UgLa3rtITh_0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP499465.RATT3gaa2E37-9Dxq778dHSJKL_oEWgT5UgLa3rtITh_0130_assertion
{
miriam-gene:10046
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGNc40b258082697c3e9496967a06662567
sio:SIO_000628
miriam-gene:10046
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP499465.RATT3gaa2E37-9Dxq778dHSJKL_oEWgT5UgLa3rtITh_0130_provenance
{
dgn-np:NP499465.RATT3gaa2E37-9Dxq778dHSJKL_oEWgT5UgLa3rtITh_0130_assertion
dcterms:description
"[To delineate the trajectories of Aβ42 level in cerebrospinal fluid (CSF), fludeoxyglucose F18 (FDG) uptake using positron emission tomography, and hippocampal volume using magnetic resonance imaging and their relative associations with cognitive change at different stages in aging and Alzheimer disease (AD).]. 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:21670386
;
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:NP499465.RATT3gaa2E37-9Dxq778dHSJKL_oEWgT5UgLa3rtITh_0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:58+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" .
}