@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1036875.RAFMq1uczpdw2rcnBfwwhxzl3CoUDYWuOUGcptPxPY-MA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1036875.RAFMq1uczpdw2rcnBfwwhxzl3CoUDYWuOUGcptPxPY-MA130_head
{
this:
np:hasAssertion
dgn-np:NP1036875.RAFMq1uczpdw2rcnBfwwhxzl3CoUDYWuOUGcptPxPY-MA130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1036875.RAFMq1uczpdw2rcnBfwwhxzl3CoUDYWuOUGcptPxPY-MA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1036875.RAFMq1uczpdw2rcnBfwwhxzl3CoUDYWuOUGcptPxPY-MA130_assertion
a
np:Assertion
.
dgn-np:NP1036875.RAFMq1uczpdw2rcnBfwwhxzl3CoUDYWuOUGcptPxPY-MA130_provenance
a
np:Provenance
.
dgn-np:NP1036875.RAFMq1uczpdw2rcnBfwwhxzl3CoUDYWuOUGcptPxPY-MA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1036875.RAFMq1uczpdw2rcnBfwwhxzl3CoUDYWuOUGcptPxPY-MA130_assertion
{
miriam-gene:116519
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN12bc3c82fbdb83d90c1115901baf68a0
sio:SIO_000628
miriam-gene:116519
,
lld:C0027051
;
a
sio:SIO_001121
.
}
dgn-np:NP1036875.RAFMq1uczpdw2rcnBfwwhxzl3CoUDYWuOUGcptPxPY-MA130_provenance
{
dgn-np:NP1036875.RAFMq1uczpdw2rcnBfwwhxzl3CoUDYWuOUGcptPxPY-MA130_assertion
dcterms:description
"[Using a Mendelian randomization approach, we tested whether genetically increased remnant cholesterol in hypertriglyceridaemia due to genetic variation in the apolipoprotein A5 gene (APOA5) associates with an increased risk of myocardial infarction (MI).]. 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:23248205
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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 .
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dgn-np:NP1036875.RAFMq1uczpdw2rcnBfwwhxzl3CoUDYWuOUGcptPxPY-MA130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
<
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> , <
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> , <
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> , <
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
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"v4.0.0" .
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