@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP52970.RAVcYa5eQHGDipwY9HpiGoAMoiQAbR4Q_G6IjD4EgbkdQ
> .
@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:NP52970.RAVcYa5eQHGDipwY9HpiGoAMoiQAbR4Q_G6IjD4EgbkdQ130_head
{
this:
np:hasAssertion
dgn-np:NP52970.RAVcYa5eQHGDipwY9HpiGoAMoiQAbR4Q_G6IjD4EgbkdQ130_assertion
;
np:hasProvenance
dgn-np:NP52970.RAVcYa5eQHGDipwY9HpiGoAMoiQAbR4Q_G6IjD4EgbkdQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP52970.RAVcYa5eQHGDipwY9HpiGoAMoiQAbR4Q_G6IjD4EgbkdQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP52970.RAVcYa5eQHGDipwY9HpiGoAMoiQAbR4Q_G6IjD4EgbkdQ130_assertion
a
np:Assertion
.
dgn-np:NP52970.RAVcYa5eQHGDipwY9HpiGoAMoiQAbR4Q_G6IjD4EgbkdQ130_provenance
a
np:Provenance
.
dgn-np:NP52970.RAVcYa5eQHGDipwY9HpiGoAMoiQAbR4Q_G6IjD4EgbkdQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP52970.RAVcYa5eQHGDipwY9HpiGoAMoiQAbR4Q_G6IjD4EgbkdQ130_assertion
{
miriam-gene:5444
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGNf8dc9e9f673e80b01fd103e286d9507b
sio:SIO_000628
miriam-gene:5444
,
lld:C0038454
;
a
sio:SIO_001122
.
}
dgn-np:NP52970.RAVcYa5eQHGDipwY9HpiGoAMoiQAbR4Q_G6IjD4EgbkdQ130_provenance
{
dgn-np:NP52970.RAVcYa5eQHGDipwY9HpiGoAMoiQAbR4Q_G6IjD4EgbkdQ130_assertion
dcterms:description
"[ These findings suggest that the PON 192RR genotype is independently associated with an increased risk of nonfatal AIS among young adults. Further studies are necessary to understand better the mechanistic implications of these observations in the development of AIS in the young.]. 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:12052975
;
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:NP52970.RAVcYa5eQHGDipwY9HpiGoAMoiQAbR4Q_G6IjD4EgbkdQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}