@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU
> .
@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:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_head
{
this:
np:hasAssertion
dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_assertion
;
np:hasProvenance
dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_provenance
;
np:hasPublicationInfo
dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_assertion
a
np:Assertion
.
dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_provenance
a
np:Provenance
.
dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_assertion
{
miriam-gene:151
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNbd052a829cec329e7aff89cc4be04a75
sio:SIO_000628
miriam-gene:151
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_provenance
{
dgn-np:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_assertion
dcterms:description
"[Our data suggest that carriers of the DD versus II genotype of the alpha(2B)-adrenoceptor are at increased risk for hypertension. The genotypic effect is most evident when comparing groups corresponding to the upper and lower tails of the blood pressure distribution in the population; however, in nondiabetic hypertensive subjects it is weakly detectable even at the population level.]. 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:14744925
;
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:NP49124.RAEKPggMEOd12uvKsV0nrk1lNQC4QMGOP00gfi3AKb8zU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}