@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4
> .
@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:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_head
{
this:
np:hasAssertion
dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_assertion
;
np:hasProvenance
dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_provenance
;
np:hasPublicationInfo
dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_assertion
a
np:Assertion
.
dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_provenance
a
np:Provenance
.
dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_assertion
{
miriam-gene:3569
a
ncit:C16612
.
lld:C0020459
a
ncit:C7057
.
dgn-gda:DGNd5f714c3cdf1ac24649573d5c93d9b71
sio:SIO_000628
miriam-gene:3569
,
lld:C0020459
;
a
sio:SIO_001121
.
}
dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_provenance
{
dgn-np:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_assertion
dcterms:description
"[Subjects homozygous for the C allele at position -174 of the IL-6 gene (SfaNI genotype), associated to lower plasma IL-6 levels, showed significantly lower integrated area under the curve of serum glucose concentrations (AUCglucose) after an oral glucose tolerance test, lower blood glycosylated hemoglobin, lower fasting insulin levels, lower total and differential white blood cell count (a putative marker of peripheral IL-6 action), and an increased insulin sensitivity index than carriers of the G allele, despite similar age and body composition.]. 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:10868978
;
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:NP799849.RACl5fENhocAyRzCASGUyq3unwFopxhA77lJSiw4RxLW4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:11+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" .
}