@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP328431.RAnymLkmuEhVeZfRQHuIsEZY6CD8Zaxiqc1aNCm3NiALM
> .
@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:NP328431.RAnymLkmuEhVeZfRQHuIsEZY6CD8Zaxiqc1aNCm3NiALM130_head
{
this:
np:hasAssertion
dgn-np:NP328431.RAnymLkmuEhVeZfRQHuIsEZY6CD8Zaxiqc1aNCm3NiALM130_assertion
;
np:hasProvenance
dgn-np:NP328431.RAnymLkmuEhVeZfRQHuIsEZY6CD8Zaxiqc1aNCm3NiALM130_provenance
;
np:hasPublicationInfo
dgn-np:NP328431.RAnymLkmuEhVeZfRQHuIsEZY6CD8Zaxiqc1aNCm3NiALM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP328431.RAnymLkmuEhVeZfRQHuIsEZY6CD8Zaxiqc1aNCm3NiALM130_assertion
a
np:Assertion
.
dgn-np:NP328431.RAnymLkmuEhVeZfRQHuIsEZY6CD8Zaxiqc1aNCm3NiALM130_provenance
a
np:Provenance
.
dgn-np:NP328431.RAnymLkmuEhVeZfRQHuIsEZY6CD8Zaxiqc1aNCm3NiALM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP328431.RAnymLkmuEhVeZfRQHuIsEZY6CD8Zaxiqc1aNCm3NiALM130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN79a648794b7618e02dfc1d67211f5acc
sio:SIO_000628
miriam-gene:348
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP328431.RAnymLkmuEhVeZfRQHuIsEZY6CD8Zaxiqc1aNCm3NiALM130_provenance
{
dgn-np:NP328431.RAnymLkmuEhVeZfRQHuIsEZY6CD8Zaxiqc1aNCm3NiALM130_assertion
dcterms:description
"[Those with any APOE epsilon4 allele in combination with atherosclerosis, peripheral vascular disease, or diabetes mellitus were at substantially higher risk of cognitive decline than those without the APOE epsilon4 allele or subclinical CVD.]. 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:10404910
;
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:NP328431.RAnymLkmuEhVeZfRQHuIsEZY6CD8Zaxiqc1aNCm3NiALM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:13+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" .
}