@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP185162.RAto0UqXVLiP92aP0isoORAlWBhwtNtvstoBH-EfUwVD8
> .
@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:NP185162.RAto0UqXVLiP92aP0isoORAlWBhwtNtvstoBH-EfUwVD8130_head
{
this:
np:hasAssertion
dgn-np:NP185162.RAto0UqXVLiP92aP0isoORAlWBhwtNtvstoBH-EfUwVD8130_assertion
;
np:hasProvenance
dgn-np:NP185162.RAto0UqXVLiP92aP0isoORAlWBhwtNtvstoBH-EfUwVD8130_provenance
;
np:hasPublicationInfo
dgn-np:NP185162.RAto0UqXVLiP92aP0isoORAlWBhwtNtvstoBH-EfUwVD8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP185162.RAto0UqXVLiP92aP0isoORAlWBhwtNtvstoBH-EfUwVD8130_assertion
a
np:Assertion
.
dgn-np:NP185162.RAto0UqXVLiP92aP0isoORAlWBhwtNtvstoBH-EfUwVD8130_provenance
a
np:Provenance
.
dgn-np:NP185162.RAto0UqXVLiP92aP0isoORAlWBhwtNtvstoBH-EfUwVD8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP185162.RAto0UqXVLiP92aP0isoORAlWBhwtNtvstoBH-EfUwVD8130_assertion
{
miriam-gene:116519
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGNc4b2222447f33e43b18b5c96b62aacdc
sio:SIO_000628
miriam-gene:116519
,
lld:C0524620
;
a
sio:SIO_001121
.
}
dgn-np:NP185162.RAto0UqXVLiP92aP0isoORAlWBhwtNtvstoBH-EfUwVD8130_provenance
{
dgn-np:NP185162.RAto0UqXVLiP92aP0isoORAlWBhwtNtvstoBH-EfUwVD8130_assertion
dcterms:description
"[Thus, the findings of the current study serve indirect evidence for the existence of rare APOA5 and GCKR haplotypes in metabolic syndrome patients with higher TG levels, which contribute to the complex lipid metabolism alteration in this disease.]. 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:21643755
;
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:NP185162.RAto0UqXVLiP92aP0isoORAlWBhwtNtvstoBH-EfUwVD8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:41+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" .
}