@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP497661.RAlxAIpQGwMjzJL_E94tkk1xPNRvEisiAR7wES0yf2UNA
> .
@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:NP497661.RAlxAIpQGwMjzJL_E94tkk1xPNRvEisiAR7wES0yf2UNA130_head
{
this:
np:hasAssertion
dgn-np:NP497661.RAlxAIpQGwMjzJL_E94tkk1xPNRvEisiAR7wES0yf2UNA130_assertion
;
np:hasProvenance
dgn-np:NP497661.RAlxAIpQGwMjzJL_E94tkk1xPNRvEisiAR7wES0yf2UNA130_provenance
;
np:hasPublicationInfo
dgn-np:NP497661.RAlxAIpQGwMjzJL_E94tkk1xPNRvEisiAR7wES0yf2UNA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP497661.RAlxAIpQGwMjzJL_E94tkk1xPNRvEisiAR7wES0yf2UNA130_assertion
a
np:Assertion
.
dgn-np:NP497661.RAlxAIpQGwMjzJL_E94tkk1xPNRvEisiAR7wES0yf2UNA130_provenance
a
np:Provenance
.
dgn-np:NP497661.RAlxAIpQGwMjzJL_E94tkk1xPNRvEisiAR7wES0yf2UNA130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP497661.RAlxAIpQGwMjzJL_E94tkk1xPNRvEisiAR7wES0yf2UNA130_assertion
{
miriam-gene:10452
a
ncit:C16612
.
lld:C0002395
a
ncit:C7057
.
dgn-gda:DGN46cb2f4d5b8a0843b28222d5d94089dc
sio:SIO_000628
miriam-gene:10452
,
lld:C0002395
;
a
sio:SIO_001121
.
}
dgn-np:NP497661.RAlxAIpQGwMjzJL_E94tkk1xPNRvEisiAR7wES0yf2UNA130_provenance
{
dgn-np:NP497661.RAlxAIpQGwMjzJL_E94tkk1xPNRvEisiAR7wES0yf2UNA130_assertion
dcterms:description
"[We report the fine mapping/sequencing results of promoter and regulatory regions of APOE cluster genes (APOE, APOC1, APOC4, APOC2, and TOMM40) in Alzheimer's disease (AD) risk as well as in the progression from mild cognitive impairment (MCI) to AD.]. 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:21752496
;
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:NP497661.RAlxAIpQGwMjzJL_E94tkk1xPNRvEisiAR7wES0yf2UNA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:57+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" .
}