@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU
> .
@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#
> .
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{
this:
np:hasAssertion
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;
np:hasProvenance
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a
np:Nanopublication
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dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_assertion
a
np:Assertion
.
dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_provenance
a
np:Provenance
.
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a
np:PublicationInfo
.
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{
miriam-gene:7984
a
ncit:C16612
.
lld:C0024141
a
ncit:C7057
.
dgn-gda:DGN47275593a31205a4066cc07dfe68127a
sio:SIO_000628
miriam-gene:7984
,
lld:C0024141
;
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.
}
dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_provenance
{
dgn-np:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_assertion
dcterms:description
"[However, it should be noted that the statistical power of our study is relatively low, which likely did not have adequate power to detect the actual correlation between the selected SNPs and SLE susceptibility; moreover, we cannot discard a possible association of other variants within the region covering TIM with SLE as a genetic risk factor, with larger samples in different populations.]. 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:21367814
;
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:NP708423.RAoRiTB3DVJLy_yAqn-SB2BIhG4WB2r-Pp92OSpSyyOpU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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
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pav:authoredBy
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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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