@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP63998.RA818Br7lXe0beg0dBdNihsxuGE49tg5kRyV-qsPeduXM
> .
@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:NP63998.RA818Br7lXe0beg0dBdNihsxuGE49tg5kRyV-qsPeduXM130_head
{
this:
np:hasAssertion
dgn-np:NP63998.RA818Br7lXe0beg0dBdNihsxuGE49tg5kRyV-qsPeduXM130_assertion
;
np:hasProvenance
dgn-np:NP63998.RA818Br7lXe0beg0dBdNihsxuGE49tg5kRyV-qsPeduXM130_provenance
;
np:hasPublicationInfo
dgn-np:NP63998.RA818Br7lXe0beg0dBdNihsxuGE49tg5kRyV-qsPeduXM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP63998.RA818Br7lXe0beg0dBdNihsxuGE49tg5kRyV-qsPeduXM130_assertion
a
np:Assertion
.
dgn-np:NP63998.RA818Br7lXe0beg0dBdNihsxuGE49tg5kRyV-qsPeduXM130_provenance
a
np:Provenance
.
dgn-np:NP63998.RA818Br7lXe0beg0dBdNihsxuGE49tg5kRyV-qsPeduXM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP63998.RA818Br7lXe0beg0dBdNihsxuGE49tg5kRyV-qsPeduXM130_assertion
{
miriam-gene:1030
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGNe76a5647ea2aba4e410cede4c864b393
sio:SIO_000628
miriam-gene:1030
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP63998.RA818Br7lXe0beg0dBdNihsxuGE49tg5kRyV-qsPeduXM130_provenance
{
dgn-np:NP63998.RA818Br7lXe0beg0dBdNihsxuGE49tg5kRyV-qsPeduXM130_assertion
dcterms:description
"[For the diabetes risk genes TCF7L2 and WFS1, which are associated with impaired incretin signaling, the level of glycemia determines SNP effects on insulin secretion. This indicates the increasing relevance of these SNPs during the progression of prediabetes stages toward clinically overt type 2 diabetes.]. 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:20802253
;
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:NP63998.RA818Br7lXe0beg0dBdNihsxuGE49tg5kRyV-qsPeduXM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:30+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" .
}