@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP236176.RAZPq1ZgRGYiKdLdlWv_0Xv6EbDjDhr8Kci9gk9uOzg_0
> .
@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:NP236176.RAZPq1ZgRGYiKdLdlWv_0Xv6EbDjDhr8Kci9gk9uOzg_0130_head
{
this:
np:hasAssertion
dgn-np:NP236176.RAZPq1ZgRGYiKdLdlWv_0Xv6EbDjDhr8Kci9gk9uOzg_0130_assertion
;
np:hasProvenance
dgn-np:NP236176.RAZPq1ZgRGYiKdLdlWv_0Xv6EbDjDhr8Kci9gk9uOzg_0130_provenance
;
np:hasPublicationInfo
dgn-np:NP236176.RAZPq1ZgRGYiKdLdlWv_0Xv6EbDjDhr8Kci9gk9uOzg_0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP236176.RAZPq1ZgRGYiKdLdlWv_0Xv6EbDjDhr8Kci9gk9uOzg_0130_assertion
a
np:Assertion
.
dgn-np:NP236176.RAZPq1ZgRGYiKdLdlWv_0Xv6EbDjDhr8Kci9gk9uOzg_0130_provenance
a
np:Provenance
.
dgn-np:NP236176.RAZPq1ZgRGYiKdLdlWv_0Xv6EbDjDhr8Kci9gk9uOzg_0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP236176.RAZPq1ZgRGYiKdLdlWv_0Xv6EbDjDhr8Kci9gk9uOzg_0130_assertion
{
miriam-gene:8741
a
ncit:C16612
.
lld:C0017661
a
ncit:C7057
.
dgn-gda:DGN04cecc2bc18218a4ef569c1d1abc3049
sio:SIO_000628
miriam-gene:8741
,
lld:C0017661
;
a
sio:SIO_001121
.
}
dgn-np:NP236176.RAZPq1ZgRGYiKdLdlWv_0Xv6EbDjDhr8Kci9gk9uOzg_0130_provenance
{
dgn-np:NP236176.RAZPq1ZgRGYiKdLdlWv_0Xv6EbDjDhr8Kci9gk9uOzg_0130_assertion
dcterms:description
"[Recent genome-wide association studies (GWAS) have identified multiple susceptibility loci for immunoglobulin A nephropathy (IgAN), the most common form of glomerulonephritis, implicating independent defects in adaptive immunity (three loci on chromosome 6p21 in the MHC region), innate immunity (8p23 DEFA locus, 17p23 TNFSF13 locus, 22q12 HORMAD2 locus), and the alternative complement pathway (1q32 CFH/CFHR locus).]. 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:23072577
;
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:NP236176.RAZPq1ZgRGYiKdLdlWv_0Xv6EbDjDhr8Kci9gk9uOzg_0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:12+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" .
}