@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP562372.RAyu4TemTtN4n-QPxnru4No0LuQKn1_dOJnbkWYRO23uc
> .
@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:NP562372.RAyu4TemTtN4n-QPxnru4No0LuQKn1_dOJnbkWYRO23uc130_head
{
this:
np:hasAssertion
dgn-np:NP562372.RAyu4TemTtN4n-QPxnru4No0LuQKn1_dOJnbkWYRO23uc130_assertion
;
np:hasProvenance
dgn-np:NP562372.RAyu4TemTtN4n-QPxnru4No0LuQKn1_dOJnbkWYRO23uc130_provenance
;
np:hasPublicationInfo
dgn-np:NP562372.RAyu4TemTtN4n-QPxnru4No0LuQKn1_dOJnbkWYRO23uc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP562372.RAyu4TemTtN4n-QPxnru4No0LuQKn1_dOJnbkWYRO23uc130_assertion
a
np:Assertion
.
dgn-np:NP562372.RAyu4TemTtN4n-QPxnru4No0LuQKn1_dOJnbkWYRO23uc130_provenance
a
np:Provenance
.
dgn-np:NP562372.RAyu4TemTtN4n-QPxnru4No0LuQKn1_dOJnbkWYRO23uc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP562372.RAyu4TemTtN4n-QPxnru4No0LuQKn1_dOJnbkWYRO23uc130_assertion
{
miriam-gene:5972
a
ncit:C16612
.
lld:C0020456
a
ncit:C7057
.
dgn-gda:DGNe65510aef3364ef9701dcd8b44d79007
sio:SIO_000628
miriam-gene:5972
,
lld:C0020456
;
a
sio:SIO_001121
.
}
dgn-np:NP562372.RAyu4TemTtN4n-QPxnru4No0LuQKn1_dOJnbkWYRO23uc130_provenance
{
dgn-np:NP562372.RAyu4TemTtN4n-QPxnru4No0LuQKn1_dOJnbkWYRO23uc130_assertion
dcterms:description
"[Because hypertension and renal hemodynamic function are also related to the risk of diabetic nephropathy and because hyperglycemia can activate the renin angiotensin system, we sought to determine if there is an association between the AGT1R polymorphism, baseline renal and peripheral hemodynamic function, and pressor response to high glucose in subjects with early uncomplicated type 1 diabetes.]. 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:10969844
;
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:NP562372.RAyu4TemTtN4n-QPxnru4No0LuQKn1_dOJnbkWYRO23uc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:39+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" .
}