@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0
> .
@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:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_head
{
this:
np:hasAssertion
dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_assertion
;
np:hasProvenance
dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_provenance
;
np:hasPublicationInfo
dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_assertion
a
np:Assertion
.
dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_provenance
a
np:Provenance
.
dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_assertion
{
miriam-gene:92086
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN2fc6141b49f48603d575d1b0067e43a8
sio:SIO_000628
miriam-gene:92086
,
lld:C0020538
;
a
sio:SIO_001121
.
}
dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_provenance
{
dgn-np:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_assertion
dcterms:description
"[These results did not support the hypothesis that the interaction between the T393C polymorphism and GGT in the association with hypertension could be caused by an indirect effect of Gs proteins mediated by glucose metabolism.]. 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:15894831
;
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:NP284486.RAQe_wFnQjoxHG4Fm_q-hYv8AdLFq_587OgQQmDdHjyl0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:40+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" .
}