@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP66244.RAz2Z6IDxzf6doM_yPfLB21ny4yjPUneslKRqd0RiVPkY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
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{
this:
np:hasAssertion
dgn-np:NP66244.RAz2Z6IDxzf6doM_yPfLB21ny4yjPUneslKRqd0RiVPkY130_assertion
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np:hasProvenance
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dgn-np:NP66244.RAz2Z6IDxzf6doM_yPfLB21ny4yjPUneslKRqd0RiVPkY130_publicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP66244.RAz2Z6IDxzf6doM_yPfLB21ny4yjPUneslKRqd0RiVPkY130_provenance
a
np:Provenance
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dgn-np:NP66244.RAz2Z6IDxzf6doM_yPfLB21ny4yjPUneslKRqd0RiVPkY130_publicationInfo
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{
miriam-gene:5444
a
ncit:C16612
.
lld:C0027051
a
ncit:C7057
.
dgn-gda:DGN373fda7dfe3d775f711be6d4f382ac11
sio:SIO_000628
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,
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;
a
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.
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dgn-np:NP66244.RAz2Z6IDxzf6doM_yPfLB21ny4yjPUneslKRqd0RiVPkY130_provenance
{
dgn-np:NP66244.RAz2Z6IDxzf6doM_yPfLB21ny4yjPUneslKRqd0RiVPkY130_assertion
dcterms:description
"[We determined the PON1-192 polymorphism by PCR-RFLP, and serum PON1 activity, using either paraoxon (PONase activity) or phenylacetate (ARE activity) as substrates, in 155 clinically healthy individuals (control group), and 155 patients with at least one myocardial infarction (CHD group).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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sio:SIO_000772
miriam-pubmed:19205543
;
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prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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
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dgn-np:NP66244.RAz2Z6IDxzf6doM_yPfLB21ny4yjPUneslKRqd0RiVPkY130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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> , <
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> , <
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> , <
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<
http://orcid.org/0000-0003-0169-8159
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