@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP90047.RAOgELMbrZVOTy1DC7Y2jMDCHUqvQ936dld7Q2F1e_oGY
> .
@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:NP90047.RAOgELMbrZVOTy1DC7Y2jMDCHUqvQ936dld7Q2F1e_oGY130_head
{
this:
np:hasAssertion
dgn-np:NP90047.RAOgELMbrZVOTy1DC7Y2jMDCHUqvQ936dld7Q2F1e_oGY130_assertion
;
np:hasProvenance
dgn-np:NP90047.RAOgELMbrZVOTy1DC7Y2jMDCHUqvQ936dld7Q2F1e_oGY130_provenance
;
np:hasPublicationInfo
dgn-np:NP90047.RAOgELMbrZVOTy1DC7Y2jMDCHUqvQ936dld7Q2F1e_oGY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP90047.RAOgELMbrZVOTy1DC7Y2jMDCHUqvQ936dld7Q2F1e_oGY130_assertion
a
np:Assertion
.
dgn-np:NP90047.RAOgELMbrZVOTy1DC7Y2jMDCHUqvQ936dld7Q2F1e_oGY130_provenance
a
np:Provenance
.
dgn-np:NP90047.RAOgELMbrZVOTy1DC7Y2jMDCHUqvQ936dld7Q2F1e_oGY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP90047.RAOgELMbrZVOTy1DC7Y2jMDCHUqvQ936dld7Q2F1e_oGY130_assertion
{
miriam-gene:1134
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN432c566dd1d4b64a6a41acefd08addb3
sio:SIO_000628
miriam-gene:1134
,
lld:C0007222
;
a
sio:SIO_001122
.
}
dgn-np:NP90047.RAOgELMbrZVOTy1DC7Y2jMDCHUqvQ936dld7Q2F1e_oGY130_provenance
{
dgn-np:NP90047.RAOgELMbrZVOTy1DC7Y2jMDCHUqvQ936dld7Q2F1e_oGY130_assertion
dcterms:description
"[CHRNG is currently thought to be expressed only during fetal development. These findings support the Barker hypothesis, that fetal genotype and intra-uterine environment influence susceptibility to chronic diseases later in life. Additional studies of this variant in other populations, as well as the effect of this variant on acetylcholine receptor expression and function, are needed to further elucidate its potential role in the regulation of blood pressure. This study suggests for the first time in humans, a possible role for genetic variation in the neuromuscular nicotinic acetylcholine receptor, particularly the gamma subunit, in systolic blood pressure regulation.]. 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:18625075
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP90047.RAOgELMbrZVOTy1DC7Y2jMDCHUqvQ936dld7Q2F1e_oGY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:44+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" .
}