@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP946601.RAG3XY9djN8mm3OzH_WqCpV5z-Sf95SLVQWo97pXbk5cg
> .
@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:NP946601.RAG3XY9djN8mm3OzH_WqCpV5z-Sf95SLVQWo97pXbk5cg130_head
{
this:
np:hasAssertion
dgn-np:NP946601.RAG3XY9djN8mm3OzH_WqCpV5z-Sf95SLVQWo97pXbk5cg130_assertion
;
np:hasProvenance
dgn-np:NP946601.RAG3XY9djN8mm3OzH_WqCpV5z-Sf95SLVQWo97pXbk5cg130_provenance
;
np:hasPublicationInfo
dgn-np:NP946601.RAG3XY9djN8mm3OzH_WqCpV5z-Sf95SLVQWo97pXbk5cg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP946601.RAG3XY9djN8mm3OzH_WqCpV5z-Sf95SLVQWo97pXbk5cg130_assertion
a
np:Assertion
.
dgn-np:NP946601.RAG3XY9djN8mm3OzH_WqCpV5z-Sf95SLVQWo97pXbk5cg130_provenance
a
np:Provenance
.
dgn-np:NP946601.RAG3XY9djN8mm3OzH_WqCpV5z-Sf95SLVQWo97pXbk5cg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP946601.RAG3XY9djN8mm3OzH_WqCpV5z-Sf95SLVQWo97pXbk5cg130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGNce0dc6796433e2cc1827250b72f46aaf
sio:SIO_000628
miriam-gene:3918
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP946601.RAG3XY9djN8mm3OzH_WqCpV5z-Sf95SLVQWo97pXbk5cg130_provenance
{
dgn-np:NP946601.RAG3XY9djN8mm3OzH_WqCpV5z-Sf95SLVQWo97pXbk5cg130_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-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:NP946601.RAG3XY9djN8mm3OzH_WqCpV5z-Sf95SLVQWo97pXbk5cg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:54+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" .
}