@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM
> .
@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:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_head
{
this:
np:hasAssertion
dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_assertion
;
np:hasProvenance
dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_provenance
;
np:hasPublicationInfo
dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_assertion
a
np:Assertion
.
dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_provenance
a
np:Provenance
.
dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_assertion
{
miriam-gene:5467
a
ncit:C16612
.
lld:C0242339
a
ncit:C7057
.
dgn-gda:DGN6a74d24ff73654497d5efa7d86434744
sio:SIO_000628
miriam-gene:5467
,
lld:C0242339
;
a
sio:SIO_001121
.
}
dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_provenance
{
dgn-np:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_assertion
dcterms:description
"[Previous studies have identified a single-nucleotide polymorphism in the gene encoding peroxisome proliferator-activated receptor-delta (PPARD), rs2016520, that is associated with changes in metabolic disease in some but not all studies, which suggests that PPARD agonists may have therapeutic benefits for the treatment of metabolic disorders, including dyslipidemia, type 2 diabetes, and obesity.]. 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:20200337
;
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:NP502705.RAi3p4PmYL-tz7YxH4KU4vfj3VXtlaLEwKjfyAFWb9elM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:59+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" .
}