@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP80995.RAbpgjXDdWoNLdyTCpSC-Z_oPc3CJ7XhrHWdrKYaEp7pI
> .
@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 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:NP80995.RAbpgjXDdWoNLdyTCpSC-Z_oPc3CJ7XhrHWdrKYaEp7pI130_head
{
this:
np:hasAssertion
dgn-np:NP80995.RAbpgjXDdWoNLdyTCpSC-Z_oPc3CJ7XhrHWdrKYaEp7pI130_assertion
;
np:hasProvenance
dgn-np:NP80995.RAbpgjXDdWoNLdyTCpSC-Z_oPc3CJ7XhrHWdrKYaEp7pI130_provenance
;
np:hasPublicationInfo
dgn-np:NP80995.RAbpgjXDdWoNLdyTCpSC-Z_oPc3CJ7XhrHWdrKYaEp7pI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80995.RAbpgjXDdWoNLdyTCpSC-Z_oPc3CJ7XhrHWdrKYaEp7pI130_assertion
a
np:Assertion
.
dgn-np:NP80995.RAbpgjXDdWoNLdyTCpSC-Z_oPc3CJ7XhrHWdrKYaEp7pI130_provenance
a
np:Provenance
.
dgn-np:NP80995.RAbpgjXDdWoNLdyTCpSC-Z_oPc3CJ7XhrHWdrKYaEp7pI130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP80995.RAbpgjXDdWoNLdyTCpSC-Z_oPc3CJ7XhrHWdrKYaEp7pI130_assertion
{
miriam-gene:6934
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGN4c4b191a45d3cc6dbcc01a6a770dc60e
sio:SIO_000628
miriam-gene:6934
,
lld:C0028754
;
a
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.
}
dgn-np:NP80995.RAbpgjXDdWoNLdyTCpSC-Z_oPc3CJ7XhrHWdrKYaEp7pI130_provenance
{
dgn-np:NP80995.RAbpgjXDdWoNLdyTCpSC-Z_oPc3CJ7XhrHWdrKYaEp7pI130_assertion
dc:description
"[Our data indicate for the first time that TCF7L2 gene variants confer an increased risk for early impairment of glucose metabolism in obese children, which is consistent with adult studies identifying TCF7L2 as a major diabetes susceptibility gene.]. 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:17311858
;
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:NP80995.RAbpgjXDdWoNLdyTCpSC-Z_oPc3CJ7XhrHWdrKYaEp7pI130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:40+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}