@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP892110.RAyWNnRDxzVXqIioKZEjiUJmzQJDZ0Flt9s50XQR1DAK8
> .
@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:NP892110.RAyWNnRDxzVXqIioKZEjiUJmzQJDZ0Flt9s50XQR1DAK8130_head
{
this:
np:hasAssertion
dgn-np:NP892110.RAyWNnRDxzVXqIioKZEjiUJmzQJDZ0Flt9s50XQR1DAK8130_assertion
;
np:hasProvenance
dgn-np:NP892110.RAyWNnRDxzVXqIioKZEjiUJmzQJDZ0Flt9s50XQR1DAK8130_provenance
;
np:hasPublicationInfo
dgn-np:NP892110.RAyWNnRDxzVXqIioKZEjiUJmzQJDZ0Flt9s50XQR1DAK8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP892110.RAyWNnRDxzVXqIioKZEjiUJmzQJDZ0Flt9s50XQR1DAK8130_assertion
a
np:Assertion
.
dgn-np:NP892110.RAyWNnRDxzVXqIioKZEjiUJmzQJDZ0Flt9s50XQR1DAK8130_provenance
a
np:Provenance
.
dgn-np:NP892110.RAyWNnRDxzVXqIioKZEjiUJmzQJDZ0Flt9s50XQR1DAK8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP892110.RAyWNnRDxzVXqIioKZEjiUJmzQJDZ0Flt9s50XQR1DAK8130_assertion
{
miriam-gene:5446
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGNd2c8e4c9906c27e184a9c423f4c0511b
sio:SIO_000628
miriam-gene:5446
,
lld:C0024141
;
a
sio:SIO_001121
.
}
dgn-np:NP892110.RAyWNnRDxzVXqIioKZEjiUJmzQJDZ0Flt9s50XQR1DAK8130_provenance
{
dgn-np:NP892110.RAyWNnRDxzVXqIioKZEjiUJmzQJDZ0Flt9s50XQR1DAK8130_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
;
sio:SIO_000772
miriam-pubmed:21223581
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP892110.RAyWNnRDxzVXqIioKZEjiUJmzQJDZ0Flt9s50XQR1DAK8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}