@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk
> .
@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:NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_head
{
this:
np:hasAssertion
dgn-np:NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_assertion
;
np:hasProvenance
dgn-np:NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_provenance
;
np:hasPublicationInfo
dgn-np:NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_assertion
a
np:Assertion
.
dgn-np:NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_provenance
a
np:Provenance
.
dgn-np:NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_assertion
{
miriam-gene:183
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGN99663ca3020dd33d5d467f3d0b0892e9
sio:SIO_000628
miriam-gene:183
,
lld:C0524620
;
a
sio:SIO_001122
.
}
dgn-np:NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_provenance
{
dgn-np:NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_assertion
dcterms:description
"[ The high MetS prevalence in Oji-Cree adults, especially women, is consistent with their high risk of T2DM and CHD. Functional polymorphisms in three candidate genes for plasma lipoproteins and blood pressure were associated with MetS in adult Oji-Cree. Furthermore, several female adolescents met the adult MetS criteria, suggesting that the genesis of MetS begins in youth, especially among aboriginal females.]. 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:15869758
;
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:NP48913.RAZGE9BJnUdq2YU9WQqkh04m7TmkRRrUZg4TZeWjzTspk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}