@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI
> .
@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:NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_head
{
this:
np:hasAssertion
dgn-np:NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_assertion
;
np:hasProvenance
dgn-np:NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance
;
np:hasPublicationInfo
dgn-np:NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_assertion
a
np:Assertion
.
dgn-np:NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance
a
np:Provenance
.
dgn-np:NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_assertion
{
miriam-gene:79068
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN219ccc5e8d64b2f3a632a919b39608e0
sio:SIO_000628
miriam-gene:79068
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_provenance
{
dgn-np:NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_assertion
dcterms:description
"[We identify T2D-associated variants in an intergenic region of chromosome 11p12, contribute to the identification of T2D-associated variants near the genes IGF2BP2 and CDKAL1 and the region of CDKN2A and CDKN2B, and confirm that variants near TCF7L2, SLC30A8, HHEX, FTO, PPARG, and KCNJ11 are associated with T2D risk.]. 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:17463248
;
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:NP64631.RA9KK04B6glIRRmcjynjw1rZb-qpebffaQ2Ab8QTg0_rI130_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" .
}