@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg
> .
@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:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_head
{
this:
np:hasAssertion
dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_assertion
;
np:hasProvenance
dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_provenance
;
np:hasPublicationInfo
dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_assertion
a
np:Assertion
.
dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_provenance
a
np:Provenance
.
dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGNf7699e76fa947931887d78c6cc8b2b19
sio:SIO_000628
miriam-gene:1437
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_provenance
{
dgn-np:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_assertion
dcterms:description
"[The observation that genetic risk variants are associated with thickness across AD-vulnerable regions of interest in CN older individuals, suggests that the combination of polygenic risk profile, neuroimaging, and CSF biomarkers may hold synergistic potential to aid in the prediction of future cognitive decline.]. 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:22169231
;
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:NP503230.RAShhvTVv-K_bF_iZM1_3obQLJpqDz3ef81L36U4NXrEg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}