@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc
> .
@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:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_head
{
this:
np:hasAssertion
dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_assertion
a
np:Assertion
.
dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_provenance
a
np:Provenance
.
dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_assertion
{
miriam-gene:847
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGNa729d84fdd93b776eec8ef791b5e68f3
sio:SIO_000628
miriam-gene:847
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_provenance
{
dgn-np:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_assertion
dcterms:description
"[Because chronic exposure to excess ROS may contribute to vascular damage, we investigated whether genetic variation in catalase was associated with susceptibility to essential hypertension (EHYT) in 324 individuals (at least 50 years old) who were randomly sampled from an isolated population living in Xiangchang, China.]. 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:11479740
;
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:NP47548.RAcb11DgYRa1dTIFFf1ngLyZM8JMFtUSv5ECouRh5fgWc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}