@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP355990.RAuRKDxvNUsK9v5DhN2FZnf4i9DNhqG6qW_OjKH7XPiYI
> .
@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:NP355990.RAuRKDxvNUsK9v5DhN2FZnf4i9DNhqG6qW_OjKH7XPiYI130_head
{
this:
np:hasAssertion
dgn-np:NP355990.RAuRKDxvNUsK9v5DhN2FZnf4i9DNhqG6qW_OjKH7XPiYI130_assertion
;
np:hasProvenance
dgn-np:NP355990.RAuRKDxvNUsK9v5DhN2FZnf4i9DNhqG6qW_OjKH7XPiYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP355990.RAuRKDxvNUsK9v5DhN2FZnf4i9DNhqG6qW_OjKH7XPiYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP355990.RAuRKDxvNUsK9v5DhN2FZnf4i9DNhqG6qW_OjKH7XPiYI130_assertion
a
np:Assertion
.
dgn-np:NP355990.RAuRKDxvNUsK9v5DhN2FZnf4i9DNhqG6qW_OjKH7XPiYI130_provenance
a
np:Provenance
.
dgn-np:NP355990.RAuRKDxvNUsK9v5DhN2FZnf4i9DNhqG6qW_OjKH7XPiYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP355990.RAuRKDxvNUsK9v5DhN2FZnf4i9DNhqG6qW_OjKH7XPiYI130_assertion
{
miriam-gene:1636
a
ncit:C16612
.
lld:C0011849
a
ncit:C7057
.
dgn-gda:DGN437e740a022af2f35d6a434031a1a4cf
sio:SIO_000628
miriam-gene:1636
,
lld:C0011849
;
a
sio:SIO_001121
.
}
dgn-np:NP355990.RAuRKDxvNUsK9v5DhN2FZnf4i9DNhqG6qW_OjKH7XPiYI130_provenance
{
dgn-np:NP355990.RAuRKDxvNUsK9v5DhN2FZnf4i9DNhqG6qW_OjKH7XPiYI130_assertion
dcterms:description
"[Because ACE insertion/deletion (I/D) polymorphism has been shown to be associated with diabetes, hypertension, coronary artery diseases, and diabetic nephropathy, and because plasma ACE concentration has been found to be associated with plasma triglyceride and total cholesterol levels in patients with type 2 diabetes, the goal of this study was to investigate whether ACE gene I/D polymorphism is associated with metabolic syndrome in Chinese subjects with type 2 diabetes.]. 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:12032106
;
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 .
}
dgn-np:NP355990.RAuRKDxvNUsK9v5DhN2FZnf4i9DNhqG6qW_OjKH7XPiYI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:26+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}