@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP374989.RAJq97mZU3Ucp9OeyPxyz3bGDcC9SbnzZGnb9bXrt29IA
> .
@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:NP374989.RAJq97mZU3Ucp9OeyPxyz3bGDcC9SbnzZGnb9bXrt29IA130_head
{
this:
np:hasAssertion
dgn-np:NP374989.RAJq97mZU3Ucp9OeyPxyz3bGDcC9SbnzZGnb9bXrt29IA130_assertion
;
np:hasProvenance
dgn-np:NP374989.RAJq97mZU3Ucp9OeyPxyz3bGDcC9SbnzZGnb9bXrt29IA130_provenance
;
np:hasPublicationInfo
dgn-np:NP374989.RAJq97mZU3Ucp9OeyPxyz3bGDcC9SbnzZGnb9bXrt29IA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP374989.RAJq97mZU3Ucp9OeyPxyz3bGDcC9SbnzZGnb9bXrt29IA130_assertion
a
np:Assertion
.
dgn-np:NP374989.RAJq97mZU3Ucp9OeyPxyz3bGDcC9SbnzZGnb9bXrt29IA130_provenance
a
np:Provenance
.
dgn-np:NP374989.RAJq97mZU3Ucp9OeyPxyz3bGDcC9SbnzZGnb9bXrt29IA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP374989.RAJq97mZU3Ucp9OeyPxyz3bGDcC9SbnzZGnb9bXrt29IA130_assertion
{
miriam-gene:1585
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGN3d99a5d04771e3471b0f63640b25d0c2
sio:SIO_000628
miriam-gene:1585
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP374989.RAJq97mZU3Ucp9OeyPxyz3bGDcC9SbnzZGnb9bXrt29IA130_provenance
{
dgn-np:NP374989.RAJq97mZU3Ucp9OeyPxyz3bGDcC9SbnzZGnb9bXrt29IA130_assertion
dcterms:description
"[The intron-2 conversion polymorphism of CYP11B2 was suggested to lead to overexpression of the gene, and may therefore have potential to predict the blood pressure response of patients with essential hypertension to angiotensin-converting enzyme inhibitors (ACEIs).]. 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:18192839
;
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:NP374989.RAJq97mZU3Ucp9OeyPxyz3bGDcC9SbnzZGnb9bXrt29IA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:39+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" .
}