@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP398519.RAB_R8tcLawaEhjJagfNeaNLf1HlGkRPQyGOrxFyb-ChQ
> .
@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:NP398519.RAB_R8tcLawaEhjJagfNeaNLf1HlGkRPQyGOrxFyb-ChQ130_head
{
this:
np:hasAssertion
dgn-np:NP398519.RAB_R8tcLawaEhjJagfNeaNLf1HlGkRPQyGOrxFyb-ChQ130_assertion
;
np:hasProvenance
dgn-np:NP398519.RAB_R8tcLawaEhjJagfNeaNLf1HlGkRPQyGOrxFyb-ChQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP398519.RAB_R8tcLawaEhjJagfNeaNLf1HlGkRPQyGOrxFyb-ChQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP398519.RAB_R8tcLawaEhjJagfNeaNLf1HlGkRPQyGOrxFyb-ChQ130_assertion
a
np:Assertion
.
dgn-np:NP398519.RAB_R8tcLawaEhjJagfNeaNLf1HlGkRPQyGOrxFyb-ChQ130_provenance
a
np:Provenance
.
dgn-np:NP398519.RAB_R8tcLawaEhjJagfNeaNLf1HlGkRPQyGOrxFyb-ChQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP398519.RAB_R8tcLawaEhjJagfNeaNLf1HlGkRPQyGOrxFyb-ChQ130_assertion
{
miriam-gene:23274
a
ncit:C16612
.
lld:C0001403
a
ncit:C7057
.
dgn-gda:DGNc8d81eedd6b45873e6d6ddd491baead5
sio:SIO_000628
miriam-gene:23274
,
lld:C0001403
;
a
sio:SIO_001121
.
}
dgn-np:NP398519.RAB_R8tcLawaEhjJagfNeaNLf1HlGkRPQyGOrxFyb-ChQ130_provenance
{
dgn-np:NP398519.RAB_R8tcLawaEhjJagfNeaNLf1HlGkRPQyGOrxFyb-ChQ130_assertion
dcterms:description
"[Two alleles at 16p13 are independently associated with the risk of Addison's disease in the Norwegian population, suggesting this chromosomal region to harbor common autoimmunity gene(s), CLEC16A and CIITA being possible independent candidates.]. 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:18593762
;
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:NP398519.RAB_R8tcLawaEhjJagfNeaNLf1HlGkRPQyGOrxFyb-ChQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:57+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" .
}