@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1085477.RAntu-92jJsQ5g0H_qX9ds-c-mqPXNtkCClzu6c2TLZ7E
> .
@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:NP1085477.RAntu-92jJsQ5g0H_qX9ds-c-mqPXNtkCClzu6c2TLZ7E130_head
{
this:
np:hasAssertion
dgn-np:NP1085477.RAntu-92jJsQ5g0H_qX9ds-c-mqPXNtkCClzu6c2TLZ7E130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP1085477.RAntu-92jJsQ5g0H_qX9ds-c-mqPXNtkCClzu6c2TLZ7E130_assertion
a
np:Assertion
.
dgn-np:NP1085477.RAntu-92jJsQ5g0H_qX9ds-c-mqPXNtkCClzu6c2TLZ7E130_provenance
a
np:Provenance
.
dgn-np:NP1085477.RAntu-92jJsQ5g0H_qX9ds-c-mqPXNtkCClzu6c2TLZ7E130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:2646
a
ncit:C16612
.
lld:C0085207
a
ncit:C7057
.
dgn-gda:DGN30560e27a6c2f88e0bc0ab5da14cf8d7
sio:SIO_000628
miriam-gene:2646
,
lld:C0085207
;
a
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.
}
dgn-np:NP1085477.RAntu-92jJsQ5g0H_qX9ds-c-mqPXNtkCClzu6c2TLZ7E130_provenance
{
dgn-np:NP1085477.RAntu-92jJsQ5g0H_qX9ds-c-mqPXNtkCClzu6c2TLZ7E130_assertion
dcterms:description
"[Additionally, risk variants rs9939609 of FTO, rs2796441 of TLE1, rs560887 of G6PC2, rs780094 of GCKR, rs7903146 of TCF7L2 and rs11708067 of ADCY5 showed nominally significant associations with GDM (OR range from 1.25 to 1.30).]. 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:23761423
;
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:NP1085477.RAntu-92jJsQ5g0H_qX9ds-c-mqPXNtkCClzu6c2TLZ7E130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:58+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
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
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> ;
pav:createdBy
<
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> ;
pav:version
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pav:version
"v4.0.0" .
}