@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP599026.RAKVqlCPAuXItZIj6Ts16mcS29vlotuha6YQD_Jwe9NSA
> .
@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:NP599026.RAKVqlCPAuXItZIj6Ts16mcS29vlotuha6YQD_Jwe9NSA130_head
{
this:
np:hasAssertion
dgn-np:NP599026.RAKVqlCPAuXItZIj6Ts16mcS29vlotuha6YQD_Jwe9NSA130_assertion
;
np:hasProvenance
dgn-np:NP599026.RAKVqlCPAuXItZIj6Ts16mcS29vlotuha6YQD_Jwe9NSA130_provenance
;
np:hasPublicationInfo
dgn-np:NP599026.RAKVqlCPAuXItZIj6Ts16mcS29vlotuha6YQD_Jwe9NSA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP599026.RAKVqlCPAuXItZIj6Ts16mcS29vlotuha6YQD_Jwe9NSA130_assertion
a
np:Assertion
.
dgn-np:NP599026.RAKVqlCPAuXItZIj6Ts16mcS29vlotuha6YQD_Jwe9NSA130_provenance
a
np:Provenance
.
dgn-np:NP599026.RAKVqlCPAuXItZIj6Ts16mcS29vlotuha6YQD_Jwe9NSA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP599026.RAKVqlCPAuXItZIj6Ts16mcS29vlotuha6YQD_Jwe9NSA130_assertion
{
miriam-gene:54832
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN791aeab32c65d0edf0c47f708b5eed50
sio:SIO_000628
miriam-gene:54832
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP599026.RAKVqlCPAuXItZIj6Ts16mcS29vlotuha6YQD_Jwe9NSA130_provenance
{
dgn-np:NP599026.RAKVqlCPAuXItZIj6Ts16mcS29vlotuha6YQD_Jwe9NSA130_assertion
dcterms:description
"[We found no detectable effect (with an OR >2.1) of the variants in GCKR, GIPR, ADCY5 and VPS13C on the response to sulfonylurea treatment, indicating that these variants are not significantly contributing to the risk of SH in patients with T2D.]. 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:22956255
;
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:NP599026.RAKVqlCPAuXItZIj6Ts16mcS29vlotuha6YQD_Jwe9NSA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:00+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" .
}