@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY
> .
@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:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_head
{
this:
np:hasAssertion
dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_assertion
;
np:hasProvenance
dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_provenance
;
np:hasPublicationInfo
dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_assertion
a
np:Assertion
.
dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_provenance
a
np:Provenance
.
dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_assertion
{
miriam-gene:5444
a
ncit:C16612
.
lld:C0020538
a
ncit:C7057
.
dgn-gda:DGN43db592d619fb65698f0c28a08e09ee0
sio:SIO_000628
miriam-gene:5444
,
lld:C0020538
;
a
sio:SIO_001122
.
}
dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_provenance
{
dgn-np:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_assertion
dcterms:description
"[The finding that PON1192RR genotype is associated with$$$ a higher prevalence of arterial hypertension may contribute to improving the stratification of cardiovascular risk within a population aged 30-60 years. Determination of the PON1192 polymorphism may help to identify those individuals who are prone to developing cardiovascular diseases at an early stage, suggesting the need for close monitoring of cardiovascular risk factors before the onset of cardiovascular disease.]. 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:16794478
;
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:NP66263.RAwQgXVwXbitEWklTtVqHzApO6ux3F_kvGLwXHntpJDqY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:31+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" .
}