@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP764222.RA9dqMVO76OJQ7sue_2AZirfTyeAfoGcTCSwuVK7nBHx0
> .
@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:NP764222.RA9dqMVO76OJQ7sue_2AZirfTyeAfoGcTCSwuVK7nBHx0130_head
{
this:
np:hasAssertion
dgn-np:NP764222.RA9dqMVO76OJQ7sue_2AZirfTyeAfoGcTCSwuVK7nBHx0130_assertion
;
np:hasProvenance
dgn-np:NP764222.RA9dqMVO76OJQ7sue_2AZirfTyeAfoGcTCSwuVK7nBHx0130_provenance
;
np:hasPublicationInfo
dgn-np:NP764222.RA9dqMVO76OJQ7sue_2AZirfTyeAfoGcTCSwuVK7nBHx0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP764222.RA9dqMVO76OJQ7sue_2AZirfTyeAfoGcTCSwuVK7nBHx0130_assertion
a
np:Assertion
.
dgn-np:NP764222.RA9dqMVO76OJQ7sue_2AZirfTyeAfoGcTCSwuVK7nBHx0130_provenance
a
np:Provenance
.
dgn-np:NP764222.RA9dqMVO76OJQ7sue_2AZirfTyeAfoGcTCSwuVK7nBHx0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP764222.RA9dqMVO76OJQ7sue_2AZirfTyeAfoGcTCSwuVK7nBHx0130_assertion
{
miriam-gene:6934
a
ncit:C16612
.
lld:C0085207
a
ncit:C7057
.
dgn-gda:DGNd3edb192ca49bed7c415e3eda4afd77b
sio:SIO_000628
miriam-gene:6934
,
lld:C0085207
;
a
sio:SIO_001121
.
}
dgn-np:NP764222.RA9dqMVO76OJQ7sue_2AZirfTyeAfoGcTCSwuVK7nBHx0130_provenance
{
dgn-np:NP764222.RA9dqMVO76OJQ7sue_2AZirfTyeAfoGcTCSwuVK7nBHx0130_assertion
dcterms:description
"[Results from current association studies on T2DM susceptible genes in GDM have shown significant heterogeneity There may be primary evidence that polymorphisms of susceptible genes of T2DM such as transcription factor 7-like 2 (TCF7L2) gene, potassium channel voltage-gate KQT-like subfamily member 1 (KCNQ1) gene, and cyclin-dependent kinase 5 regulatory subunit-associated protein 1-like 1 (CDKAL1) gene, may increase risk of GDM.]. 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:22891507
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP764222.RA9dqMVO76OJQ7sue_2AZirfTyeAfoGcTCSwuVK7nBHx0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:42+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" .
}