@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0
> .
@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 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:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_head
{
this:
np:hasAssertion
dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_assertion
;
np:hasProvenance
dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_provenance
;
np:hasPublicationInfo
dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_assertion
a
np:Assertion
.
dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_provenance
a
np:Provenance
.
dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_assertion
{
miriam-gene:7391
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGNe76ff313a46ad350516d9c8ca4095ab2
sio:SIO_000628
miriam-gene:7391
,
lld:C0524620
;
a
sio:SIO_001122
.
}
dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_provenance
{
dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_assertion
dc:description
"[Seven APOA5 single nucleotide polymorphisms (SNPs) were analyzed in combination with six USF1 SNPs, applying logistic regression in an additive model adjusting for age and sex and the definition for metabolic syndrome from the National Cholesterol Education Program's Adult Treatment Panel III (NCEP (AIII)) including medication.]. 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:20054229
;
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 .
}
dgn-np:NP79987.RAcE3bo1o8Ihbqyghb_kCrAlJvQDJLAkdFa3EMnexLfu0130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:39+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}