@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP529306.RAQ70o9HwsAwiko2f_RnHRiN5iFpB83SbH0m3ENYmG39M
> .
@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:NP529306.RAQ70o9HwsAwiko2f_RnHRiN5iFpB83SbH0m3ENYmG39M130_head
{
this:
np:hasAssertion
dgn-np:NP529306.RAQ70o9HwsAwiko2f_RnHRiN5iFpB83SbH0m3ENYmG39M130_assertion
;
np:hasProvenance
dgn-np:NP529306.RAQ70o9HwsAwiko2f_RnHRiN5iFpB83SbH0m3ENYmG39M130_provenance
;
np:hasPublicationInfo
dgn-np:NP529306.RAQ70o9HwsAwiko2f_RnHRiN5iFpB83SbH0m3ENYmG39M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP529306.RAQ70o9HwsAwiko2f_RnHRiN5iFpB83SbH0m3ENYmG39M130_assertion
a
np:Assertion
.
dgn-np:NP529306.RAQ70o9HwsAwiko2f_RnHRiN5iFpB83SbH0m3ENYmG39M130_provenance
a
np:Provenance
.
dgn-np:NP529306.RAQ70o9HwsAwiko2f_RnHRiN5iFpB83SbH0m3ENYmG39M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP529306.RAQ70o9HwsAwiko2f_RnHRiN5iFpB83SbH0m3ENYmG39M130_assertion
{
miriam-gene:43
a
ncit:C16612
.
lld:C0020473
a
ncit:C7057
.
dgn-gda:DGN00060539b9b2fd8e4111824160b65ba5
sio:SIO_000628
miriam-gene:43
,
lld:C0020473
;
a
sio:SIO_001121
.
}
dgn-np:NP529306.RAQ70o9HwsAwiko2f_RnHRiN5iFpB83SbH0m3ENYmG39M130_provenance
{
dgn-np:NP529306.RAQ70o9HwsAwiko2f_RnHRiN5iFpB83SbH0m3ENYmG39M130_assertion
dcterms:description
"[The inheritance of the apolipoprotein E4 (APOE4) allele has been shown to increase the plasma cholesterol level, but little information is as concerns the association of the APOE genotype and hyperlipidaemia and the activities of two serum enzymes, acetylcholinesterase (AChE) and butyrylcholinesterase (BChE).]. 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:15219807
;
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:NP529306.RAQ70o9HwsAwiko2f_RnHRiN5iFpB83SbH0m3ENYmG39M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:20+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" .
}