@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_assertion
a
np:Assertion
.
dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_provenance
a
np:Provenance
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dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_publicationInfo
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np:PublicationInfo
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{
miriam-gene:55937
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN003ce28dd73ff825b2883213fde6fc33
sio:SIO_000628
miriam-gene:55937
,
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;
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.
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dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_provenance
{
dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_assertion
dcterms:description
"[The present study provided the first evidence that SNP T-778C in the proximal promoter region of apoM gene was associated with the levels of plasma CHO and FPG and also conferred the risk in the development of T2D among Han Chinese.]. 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:16572495
;
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 .
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dgn-np:NP63696.RATF2op6T3EwfgVg-syzAWTgRUEm4cIxFVw488whQfIYk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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
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<
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> , <
http://orcid.org/0000-0002-7534-7661
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> , <
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> , <
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> ;
pav:createdBy
<
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> ;
pav:version
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