@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP338968.RAuHIOr8yfmQsX7T4gDPVrDHVfYfGS8fKX8nI3Xv46PfA
> .
@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:NP338968.RAuHIOr8yfmQsX7T4gDPVrDHVfYfGS8fKX8nI3Xv46PfA130_head
{
this:
np:hasAssertion
dgn-np:NP338968.RAuHIOr8yfmQsX7T4gDPVrDHVfYfGS8fKX8nI3Xv46PfA130_assertion
;
np:hasProvenance
dgn-np:NP338968.RAuHIOr8yfmQsX7T4gDPVrDHVfYfGS8fKX8nI3Xv46PfA130_provenance
;
np:hasPublicationInfo
dgn-np:NP338968.RAuHIOr8yfmQsX7T4gDPVrDHVfYfGS8fKX8nI3Xv46PfA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP338968.RAuHIOr8yfmQsX7T4gDPVrDHVfYfGS8fKX8nI3Xv46PfA130_assertion
a
np:Assertion
.
dgn-np:NP338968.RAuHIOr8yfmQsX7T4gDPVrDHVfYfGS8fKX8nI3Xv46PfA130_provenance
a
np:Provenance
.
dgn-np:NP338968.RAuHIOr8yfmQsX7T4gDPVrDHVfYfGS8fKX8nI3Xv46PfA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP338968.RAuHIOr8yfmQsX7T4gDPVrDHVfYfGS8fKX8nI3Xv46PfA130_assertion
{
miriam-gene:185
a
ncit:C16612
.
lld:C0085580
a
ncit:C7057
.
dgn-gda:DGNf464405628ff7cef715ed0ea40a68a38
sio:SIO_000628
miriam-gene:185
,
lld:C0085580
;
a
sio:SIO_001121
.
}
dgn-np:NP338968.RAuHIOr8yfmQsX7T4gDPVrDHVfYfGS8fKX8nI3Xv46PfA130_provenance
{
dgn-np:NP338968.RAuHIOr8yfmQsX7T4gDPVrDHVfYfGS8fKX8nI3Xv46PfA130_assertion
dcterms:description
"[The angiotensin II type 1 receptor (AT-1) mediates the major pressor and trophic actions of angiotensin II (Ang II) and at least 50 different polymorphisms have been described in the AT-1 gene (AT(1)R gene); in particular, the C allele of the +1166A/C polymorphism has been associated with the severe form of essential hypertension, but the role of this polymorphism is still ambiguous in pathologies related to high Ang II levels, such as deterioration of renal function, arterial stiffness and hypertrophic cardiomyopathy.]. 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:15640279
;
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:NP338968.RAuHIOr8yfmQsX7T4gDPVrDHVfYfGS8fKX8nI3Xv46PfA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:19+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" .
}