@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1001135.RAF2ibOVc7SHoKZAHhoQnljxSRPPFWNnAUA87AisGzbSI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1001135.RAF2ibOVc7SHoKZAHhoQnljxSRPPFWNnAUA87AisGzbSI130_head
{
this:
np:hasAssertion
dgn-np:NP1001135.RAF2ibOVc7SHoKZAHhoQnljxSRPPFWNnAUA87AisGzbSI130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1001135.RAF2ibOVc7SHoKZAHhoQnljxSRPPFWNnAUA87AisGzbSI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1001135.RAF2ibOVc7SHoKZAHhoQnljxSRPPFWNnAUA87AisGzbSI130_assertion
a
np:Assertion
.
dgn-np:NP1001135.RAF2ibOVc7SHoKZAHhoQnljxSRPPFWNnAUA87AisGzbSI130_provenance
a
np:Provenance
.
dgn-np:NP1001135.RAF2ibOVc7SHoKZAHhoQnljxSRPPFWNnAUA87AisGzbSI130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP1001135.RAF2ibOVc7SHoKZAHhoQnljxSRPPFWNnAUA87AisGzbSI130_assertion
{
miriam-gene:6934
a
ncit:C16612
.
lld:C0035309
a
ncit:C7057
.
dgn-gda:DGNc957bbbe150a48003c8855cf92e3b9ce
sio:SIO_000628
miriam-gene:6934
,
lld:C0035309
;
a
sio:SIO_001121
.
}
dgn-np:NP1001135.RAF2ibOVc7SHoKZAHhoQnljxSRPPFWNnAUA87AisGzbSI130_provenance
{
dgn-np:NP1001135.RAF2ibOVc7SHoKZAHhoQnljxSRPPFWNnAUA87AisGzbSI130_assertion
dcterms:description
"[In conclusion, our study, in addition to confirming the involvement of TCF7L2 gene in the T2DM susceptibility, has shown that TCF7L2 genetic variability also contributes to the development of diabetic complications such as retinopathy and cardiovascular autonomic neuropathy.]. 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:22843023
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1001135.RAF2ibOVc7SHoKZAHhoQnljxSRPPFWNnAUA87AisGzbSI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:19+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
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;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}