@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP376620.RA0yV5AD8ju1Dw-C8m06E66nMpI-TyKtYVTu8eqUVTpKA
> .
@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:NP376620.RA0yV5AD8ju1Dw-C8m06E66nMpI-TyKtYVTu8eqUVTpKA130_head
{
this:
np:hasAssertion
dgn-np:NP376620.RA0yV5AD8ju1Dw-C8m06E66nMpI-TyKtYVTu8eqUVTpKA130_assertion
;
np:hasProvenance
dgn-np:NP376620.RA0yV5AD8ju1Dw-C8m06E66nMpI-TyKtYVTu8eqUVTpKA130_provenance
;
np:hasPublicationInfo
dgn-np:NP376620.RA0yV5AD8ju1Dw-C8m06E66nMpI-TyKtYVTu8eqUVTpKA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP376620.RA0yV5AD8ju1Dw-C8m06E66nMpI-TyKtYVTu8eqUVTpKA130_assertion
a
np:Assertion
.
dgn-np:NP376620.RA0yV5AD8ju1Dw-C8m06E66nMpI-TyKtYVTu8eqUVTpKA130_provenance
a
np:Provenance
.
dgn-np:NP376620.RA0yV5AD8ju1Dw-C8m06E66nMpI-TyKtYVTu8eqUVTpKA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP376620.RA0yV5AD8ju1Dw-C8m06E66nMpI-TyKtYVTu8eqUVTpKA130_assertion
{
miriam-gene:4544
a
ncit:C16612
.
lld:C0020456
a
ncit:C7057
.
dgn-gda:DGNca65bcab1f3551b32bedb12e54aa3f9a
sio:SIO_000628
miriam-gene:4544
,
lld:C0020456
;
a
sio:SIO_001121
.
}
dgn-np:NP376620.RA0yV5AD8ju1Dw-C8m06E66nMpI-TyKtYVTu8eqUVTpKA130_provenance
{
dgn-np:NP376620.RA0yV5AD8ju1Dw-C8m06E66nMpI-TyKtYVTu8eqUVTpKA130_assertion
dcterms:description
"[Common variants of MTNR1B, G6PC2 and GCK are associated with elevated FPG and impaired insulin secretion, both individually and jointly, suggesting that these risk alleles may precipitate or perpetuate hyperglycemia in predisposed individuals.]. 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:20628598
;
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:NP376620.RA0yV5AD8ju1Dw-C8m06E66nMpI-TyKtYVTu8eqUVTpKA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:40+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" .
}