@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP200696.RAlaFezX9HRcOxLA3aWPISIbisoudA7yzr4MKvBSE3VfI
> .
@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:NP200696.RAlaFezX9HRcOxLA3aWPISIbisoudA7yzr4MKvBSE3VfI130_head
{
this:
np:hasAssertion
dgn-np:NP200696.RAlaFezX9HRcOxLA3aWPISIbisoudA7yzr4MKvBSE3VfI130_assertion
;
np:hasProvenance
dgn-np:NP200696.RAlaFezX9HRcOxLA3aWPISIbisoudA7yzr4MKvBSE3VfI130_provenance
;
np:hasPublicationInfo
dgn-np:NP200696.RAlaFezX9HRcOxLA3aWPISIbisoudA7yzr4MKvBSE3VfI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP200696.RAlaFezX9HRcOxLA3aWPISIbisoudA7yzr4MKvBSE3VfI130_assertion
a
np:Assertion
.
dgn-np:NP200696.RAlaFezX9HRcOxLA3aWPISIbisoudA7yzr4MKvBSE3VfI130_provenance
a
np:Provenance
.
dgn-np:NP200696.RAlaFezX9HRcOxLA3aWPISIbisoudA7yzr4MKvBSE3VfI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP200696.RAlaFezX9HRcOxLA3aWPISIbisoudA7yzr4MKvBSE3VfI130_assertion
{
miriam-gene:1071
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGN0ae96ed0c3fbfd8c92b3f6f5ab3921da
sio:SIO_000628
miriam-gene:1071
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP200696.RAlaFezX9HRcOxLA3aWPISIbisoudA7yzr4MKvBSE3VfI130_provenance
{
dgn-np:NP200696.RAlaFezX9HRcOxLA3aWPISIbisoudA7yzr4MKvBSE3VfI130_assertion
dcterms:description
"[Using data from two ongoing epidemiologic clinical-pathologic cohort studies of aging and dementia in the United States, the Religious Order Study and the Memory and Aging Project, we evaluated the association of the CETP I405V polymorphism (rs5882) with cognitive decline and risk of incident AD in more than 1300 participants of European ancestry.]. 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:22122979
;
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:NP200696.RAlaFezX9HRcOxLA3aWPISIbisoudA7yzr4MKvBSE3VfI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:50+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" .
}