@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM
> .
@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:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_head
{
this:
np:hasAssertion
dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_assertion
;
np:hasProvenance
dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_provenance
;
np:hasPublicationInfo
dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_assertion
a
np:Assertion
.
dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_provenance
a
np:Provenance
.
dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_assertion
{
miriam-gene:22925
a
ncit:C16612
.
lld:C0017665
a
ncit:C7057
.
dgn-gda:DGN18aac82b2c11973582814ccb8e29d219
sio:SIO_000628
miriam-gene:22925
,
lld:C0017665
;
a
sio:SIO_001122
.
}
dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_provenance
{
dgn-np:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_assertion
dcterms:description
"[An HLA-DQA1 allele on chromosome 6p21 is most closely associated with idiopathic membranous nephropathy in persons of white ancestry. This allele may facilitate an autoimmune response against targets such as variants of PLA2R1. Our findings suggest a basis for understanding this disease and illuminate how adaptive immunity is regulated by HLA.]. 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:21323541
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP95784.RADj09VPNJrWmQNqb-t8-G6v_p_tJCg5mNX-nJLYlWyCM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:47+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" .
}