@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP242726.RAb51bZ11T5G5Y7CqL6oAthb8e4Zdizq-VBhbQiTMLSRw
> .
@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:NP242726.RAb51bZ11T5G5Y7CqL6oAthb8e4Zdizq-VBhbQiTMLSRw130_head
{
this:
np:hasAssertion
dgn-np:NP242726.RAb51bZ11T5G5Y7CqL6oAthb8e4Zdizq-VBhbQiTMLSRw130_assertion
;
np:hasProvenance
dgn-np:NP242726.RAb51bZ11T5G5Y7CqL6oAthb8e4Zdizq-VBhbQiTMLSRw130_provenance
;
np:hasPublicationInfo
dgn-np:NP242726.RAb51bZ11T5G5Y7CqL6oAthb8e4Zdizq-VBhbQiTMLSRw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP242726.RAb51bZ11T5G5Y7CqL6oAthb8e4Zdizq-VBhbQiTMLSRw130_assertion
a
np:Assertion
.
dgn-np:NP242726.RAb51bZ11T5G5Y7CqL6oAthb8e4Zdizq-VBhbQiTMLSRw130_provenance
a
np:Provenance
.
dgn-np:NP242726.RAb51bZ11T5G5Y7CqL6oAthb8e4Zdizq-VBhbQiTMLSRw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP242726.RAb51bZ11T5G5Y7CqL6oAthb8e4Zdizq-VBhbQiTMLSRw130_assertion
{
miriam-gene:3557
a
ncit:C16612
.
lld:C0151436
a
ncit:C7057
.
dgn-gda:DGNa2d417b9587325c7a4aa9c1d9b9bcaa3
sio:SIO_000628
miriam-gene:3557
,
lld:C0151436
;
a
sio:SIO_001121
.
}
dgn-np:NP242726.RAb51bZ11T5G5Y7CqL6oAthb8e4Zdizq-VBhbQiTMLSRw130_provenance
{
dgn-np:NP242726.RAb51bZ11T5G5Y7CqL6oAthb8e4Zdizq-VBhbQiTMLSRw130_assertion
dcterms:description
"[To assess the influence of interleukin 1 receptor antagonist gene polymorphism (IL1RN) in the incidence of Henoch-Schönlein purpura (HSP) and cutaneous leukocytoclastic angiitis (CLA) and to determine if implications exist with severe systemic complications of HSP, in particular with severe renal involvement and permanent renal dysfunction (renal sequelae).]. 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:12136897
;
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:NP242726.RAb51bZ11T5G5Y7CqL6oAthb8e4Zdizq-VBhbQiTMLSRw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:16+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" .
}