@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_assertion
;
np:hasProvenance
dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_provenance
;
np:hasPublicationInfo
dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_assertion
a
np:Assertion
.
dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_provenance
a
np:Provenance
.
dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_assertion
{
miriam-gene:8301
a
ncit:C16612
.
lld:C0011265
a
ncit:C7057
.
dgn-gda:DGN6233839b8e075afd4638a21d2ce5a4d8
sio:SIO_000628
miriam-gene:8301
,
lld:C0011265
;
a
sio:SIO_001121
.
}
dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_provenance
{
dgn-np:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_assertion
dcterms:description
"[The associated region extends 120 kb encompassing 11 candidate genes.While AGER encodes a key receptor for amyloid-β protein, an analysis of network context based upon genes now confirmed to contribute to dementia risk (AβPP, PSEN1, PSEN2, CR1, CLU, PICALM, and APOE) suggested strong functional coupling to NOTCH4, with no significant coupling to the remaining candidates.]. 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:21297263
;
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:NP627537.RAnqGaOEGMpxp-wCCSLnpJp9D0elrkXWz9QW4g6TKgjjY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:18+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
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
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> ;
pav:version
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}