@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI
> .
@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:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_head
{
this:
np:hasAssertion
dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_assertion
;
np:hasProvenance
dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_provenance
;
np:hasPublicationInfo
dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_assertion
a
np:Assertion
.
dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_provenance
a
np:Provenance
.
dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_assertion
{
miriam-gene:3162
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN6224af4ce74f9811e26ab316c8521efa
sio:SIO_000628
miriam-gene:3162
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_provenance
{
dgn-np:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_assertion
dcterms:description
"[ The AA genotype of HMOX-1 is associated with an increased incidence of hypertension in women. Oestrogen attenuates vasoconstriction by increasing the expression of inducible nitric oxide synthase. As carbon monoxide, which is one of the products of HO-1, can attenuate nitric oxide-induced vasodilatation, a high expression of HO-1 may cause hypertension, especially in women.]. 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:12872043
;
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:NP57588.RAB4EFcvaS9cRmSjO_TDSVlQMHRjEaYKk0P37YnHK7QrI130_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" .
}