@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI
> .
@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:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_head
{
this:
np:hasAssertion
dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_assertion
;
np:hasProvenance
dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_provenance
;
np:hasPublicationInfo
dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_assertion
a
np:Assertion
.
dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_provenance
a
np:Provenance
.
dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0007820
a
ncit:C7057
.
dgn-gda:DGN33759efa1819460167b000e1973331d1
sio:SIO_000628
miriam-gene:348
,
lld:C0007820
;
a
sio:SIO_001122
.
}
dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_provenance
{
dgn-np:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_assertion
dcterms:description
"[The apoE4 allele exacerbates the effects of cerebrovascular risk factors on NP function. This relationship appears to be driven by SBP, suggesting that treatment of high SBP could potentially reduce risk of cognitive impairment among those already at increased risk for Alzheimer disease.]. 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:20471857
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48257.RAAsoPrxxyzxBX_VhI6Yn5_-5V4W44mpNgcKjlNT8tmUI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}