@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP189181.RAOUjNID8N4VrJKAW9cXOcepuXg1lKHQofMgIL-xX1wiE
> .
@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/v4.0.0/void/
> .
dgn-np:NP189181.RAOUjNID8N4VrJKAW9cXOcepuXg1lKHQofMgIL-xX1wiE130_head
{
this:
np:hasAssertion
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;
np:hasProvenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP189181.RAOUjNID8N4VrJKAW9cXOcepuXg1lKHQofMgIL-xX1wiE130_assertion
a
np:Assertion
.
dgn-np:NP189181.RAOUjNID8N4VrJKAW9cXOcepuXg1lKHQofMgIL-xX1wiE130_provenance
a
np:Provenance
.
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a
np:PublicationInfo
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{
miriam-gene:5446
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN8863166a195497f94ca7f276ec62fe30
sio:SIO_000628
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,
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;
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.
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dgn-np:NP189181.RAOUjNID8N4VrJKAW9cXOcepuXg1lKHQofMgIL-xX1wiE130_provenance
{
dgn-np:NP189181.RAOUjNID8N4VrJKAW9cXOcepuXg1lKHQofMgIL-xX1wiE130_assertion
dcterms:description
"[Since PON1, PON2 and PON3 share high degree of structural and functional properties, in this study, we examined the role of PON2 genetic variation on serum PON activity, risk of SLE and SLE-related clinical manifestations in a Caucasian case-control sample.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:21223581
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
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
"DisGeNET evidence - LITERATURE"@en .
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dgn-np:NP189181.RAOUjNID8N4VrJKAW9cXOcepuXg1lKHQofMgIL-xX1wiE130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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;
pav:authoredBy
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> , <
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> , <
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> , <
http://orcid.org/0000-0003-0169-8159
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> ;
pav:createdBy
<
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