@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP425102.RABqbmC_3CbTtB27__doJ5cx4vcfQV7J0iOhdGDkAMjVw
> .
@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:NP425102.RABqbmC_3CbTtB27__doJ5cx4vcfQV7J0iOhdGDkAMjVw130_head
{
this:
np:hasAssertion
dgn-np:NP425102.RABqbmC_3CbTtB27__doJ5cx4vcfQV7J0iOhdGDkAMjVw130_assertion
;
np:hasProvenance
dgn-np:NP425102.RABqbmC_3CbTtB27__doJ5cx4vcfQV7J0iOhdGDkAMjVw130_provenance
;
np:hasPublicationInfo
dgn-np:NP425102.RABqbmC_3CbTtB27__doJ5cx4vcfQV7J0iOhdGDkAMjVw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP425102.RABqbmC_3CbTtB27__doJ5cx4vcfQV7J0iOhdGDkAMjVw130_assertion
a
np:Assertion
.
dgn-np:NP425102.RABqbmC_3CbTtB27__doJ5cx4vcfQV7J0iOhdGDkAMjVw130_provenance
a
np:Provenance
.
dgn-np:NP425102.RABqbmC_3CbTtB27__doJ5cx4vcfQV7J0iOhdGDkAMjVw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP425102.RABqbmC_3CbTtB27__doJ5cx4vcfQV7J0iOhdGDkAMjVw130_assertion
{
miriam-gene:185
a
ncit:C16612
.
lld:C0007194
a
ncit:C7057
.
dgn-gda:DGN44727fa0d570c0d713719165beafee25
sio:SIO_000628
miriam-gene:185
,
lld:C0007194
;
a
sio:SIO_001121
.
}
dgn-np:NP425102.RABqbmC_3CbTtB27__doJ5cx4vcfQV7J0iOhdGDkAMjVw130_provenance
{
dgn-np:NP425102.RABqbmC_3CbTtB27__doJ5cx4vcfQV7J0iOhdGDkAMjVw130_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:NP425102.RABqbmC_3CbTtB27__doJ5cx4vcfQV7J0iOhdGDkAMjVw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:12+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" .
}