@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE
> .
@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:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_head
{
this:
np:hasAssertion
dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_assertion
;
np:hasProvenance
dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_provenance
;
np:hasPublicationInfo
dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_assertion
a
np:Assertion
.
dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_provenance
a
np:Provenance
.
dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_assertion
{
miriam-gene:348
a
ncit:C16612
.
lld:C0520679
a
ncit:C7057
.
dgn-gda:DGNf56db38aaeb1995c5a4d1b19e73b8652
sio:SIO_000628
miriam-gene:348
,
lld:C0520679
;
a
sio:SIO_001122
.
}
dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_provenance
{
dgn-np:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_assertion
dcterms:description
"[APOE epsilon4 allele is more frequent in children with obstructive sleep apnea and particularly in those who develop neurocognitive deficits, suggesting that the APOE epsilon4 allele is associated with not only increased odds of having sleep-disordered breathing, but also with an increased risk for neurocognitive dysfunction.]. 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:17636061
;
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:NP86035.RAmeQMzkg67X5TS_GtJLIyunZQS8SkWX-tz3Kk2O21caE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:42+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" .
}