@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61186.RAPcv-KO8QOeXpOWVtH0gn6HUppFCq-P_YgVur-6ITJ8E
> .
@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:NP61186.RAPcv-KO8QOeXpOWVtH0gn6HUppFCq-P_YgVur-6ITJ8E130_head
{
this:
np:hasAssertion
dgn-np:NP61186.RAPcv-KO8QOeXpOWVtH0gn6HUppFCq-P_YgVur-6ITJ8E130_assertion
;
np:hasProvenance
dgn-np:NP61186.RAPcv-KO8QOeXpOWVtH0gn6HUppFCq-P_YgVur-6ITJ8E130_provenance
;
np:hasPublicationInfo
dgn-np:NP61186.RAPcv-KO8QOeXpOWVtH0gn6HUppFCq-P_YgVur-6ITJ8E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61186.RAPcv-KO8QOeXpOWVtH0gn6HUppFCq-P_YgVur-6ITJ8E130_assertion
a
np:Assertion
.
dgn-np:NP61186.RAPcv-KO8QOeXpOWVtH0gn6HUppFCq-P_YgVur-6ITJ8E130_provenance
a
np:Provenance
.
dgn-np:NP61186.RAPcv-KO8QOeXpOWVtH0gn6HUppFCq-P_YgVur-6ITJ8E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61186.RAPcv-KO8QOeXpOWVtH0gn6HUppFCq-P_YgVur-6ITJ8E130_assertion
{
miriam-gene:3953
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN217c5fe5daa9ac63007e885305b2f72f
sio:SIO_000628
miriam-gene:3953
,
lld:C0011860
;
a
sio:SIO_001122
.
}
dgn-np:NP61186.RAPcv-KO8QOeXpOWVtH0gn6HUppFCq-P_YgVur-6ITJ8E130_provenance
{
dgn-np:NP61186.RAPcv-KO8QOeXpOWVtH0gn6HUppFCq-P_YgVur-6ITJ8E130_assertion
dcterms:description
"[Variants located within the gene TCF7L2 are strongly associated with T2D but not with MS, providing support to previous evidence indicating that polymorphisms at the TCF7L2 gene increase T2D risk. In contrast, the non-synonymous ADRB3 rs4994 polymorphism is associated with T2D and MS.]. 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:20503258
;
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:NP61186.RAPcv-KO8QOeXpOWVtH0gn6HUppFCq-P_YgVur-6ITJ8E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}