@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP330283.RAObSRmPzScnKHmVYSQP21Vq2zT_WDZUxV6ulX8eGR50I
> .
@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:NP330283.RAObSRmPzScnKHmVYSQP21Vq2zT_WDZUxV6ulX8eGR50I130_head
{
this:
np:hasAssertion
dgn-np:NP330283.RAObSRmPzScnKHmVYSQP21Vq2zT_WDZUxV6ulX8eGR50I130_assertion
;
np:hasProvenance
dgn-np:NP330283.RAObSRmPzScnKHmVYSQP21Vq2zT_WDZUxV6ulX8eGR50I130_provenance
;
np:hasPublicationInfo
dgn-np:NP330283.RAObSRmPzScnKHmVYSQP21Vq2zT_WDZUxV6ulX8eGR50I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP330283.RAObSRmPzScnKHmVYSQP21Vq2zT_WDZUxV6ulX8eGR50I130_assertion
a
np:Assertion
.
dgn-np:NP330283.RAObSRmPzScnKHmVYSQP21Vq2zT_WDZUxV6ulX8eGR50I130_provenance
a
np:Provenance
.
dgn-np:NP330283.RAObSRmPzScnKHmVYSQP21Vq2zT_WDZUxV6ulX8eGR50I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP330283.RAObSRmPzScnKHmVYSQP21Vq2zT_WDZUxV6ulX8eGR50I130_assertion
{
miriam-gene:2645
a
ncit:C16612
.
lld:C0085207
a
ncit:C7057
.
dgn-gda:DGN3d0ae7da0499134e6acc0e743482a789
sio:SIO_000628
miriam-gene:2645
,
lld:C0085207
;
a
sio:SIO_001121
.
}
dgn-np:NP330283.RAObSRmPzScnKHmVYSQP21Vq2zT_WDZUxV6ulX8eGR50I130_provenance
{
dgn-np:NP330283.RAObSRmPzScnKHmVYSQP21Vq2zT_WDZUxV6ulX8eGR50I130_assertion
dcterms:description
"[Hyperglycemia and Adverse Pregnancy Outcome (HAPO) study: common genetic variants in GCK and TCF7L2 are associated with fasting and postchallenge glucose levels in pregnancy and with the new consensus definition of gestational diabetes mellitus from the International Association of Diabetes and Pregnancy Study Groups.]. 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:20682688
;
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:NP330283.RAObSRmPzScnKHmVYSQP21Vq2zT_WDZUxV6ulX8eGR50I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:14+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" .
}