@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg
> .
@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:NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_head
{
this:
np:hasAssertion
dgn-np:NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_assertion
;
np:hasProvenance
dgn-np:NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_provenance
;
np:hasPublicationInfo
dgn-np:NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_assertion
a
np:Assertion
.
dgn-np:NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_provenance
a
np:Provenance
.
dgn-np:NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_assertion
{
miriam-gene:3291
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN66c68008b87040441a328942af07ccfa
sio:SIO_000628
miriam-gene:3291
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_provenance
{
dgn-np:NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_assertion
dcterms:description
"[ Two different polymorphisms of the HSD11B2 gene were observed. The association of both polymorphisms was significantly higher in hypertensive subjects than in control subjects. Its role should be further investigated, but it could be related to other mutations in the promoter region of HSD11B2 or to the modulation of 11beta-HSD2 mRNA processing in hypertensive subjects.]. 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:16109323
;
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:NP57529.RAuJWcMXGMveBZcIwWXUFHT34OrC6XLzTmiXpP9c-mMDg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}