@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP538466.RAEDzip6anXX06vQYxbvmc2kBlam9n1cBEbwATJ4Bul04
> .
@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:NP538466.RAEDzip6anXX06vQYxbvmc2kBlam9n1cBEbwATJ4Bul04130_head
{
this:
np:hasAssertion
dgn-np:NP538466.RAEDzip6anXX06vQYxbvmc2kBlam9n1cBEbwATJ4Bul04130_assertion
;
np:hasProvenance
dgn-np:NP538466.RAEDzip6anXX06vQYxbvmc2kBlam9n1cBEbwATJ4Bul04130_provenance
;
np:hasPublicationInfo
dgn-np:NP538466.RAEDzip6anXX06vQYxbvmc2kBlam9n1cBEbwATJ4Bul04130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP538466.RAEDzip6anXX06vQYxbvmc2kBlam9n1cBEbwATJ4Bul04130_assertion
a
np:Assertion
.
dgn-np:NP538466.RAEDzip6anXX06vQYxbvmc2kBlam9n1cBEbwATJ4Bul04130_provenance
a
np:Provenance
.
dgn-np:NP538466.RAEDzip6anXX06vQYxbvmc2kBlam9n1cBEbwATJ4Bul04130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP538466.RAEDzip6anXX06vQYxbvmc2kBlam9n1cBEbwATJ4Bul04130_assertion
{
miriam-gene:7133
a
ncit:C16612
.
lld:C0042384
a
ncit:C7057
.
dgn-gda:DGNc369a46f081eed5a590b81b9a31eb851
sio:SIO_000628
miriam-gene:7133
,
lld:C0042384
;
a
sio:SIO_001121
.
}
dgn-np:NP538466.RAEDzip6anXX06vQYxbvmc2kBlam9n1cBEbwATJ4Bul04130_provenance
{
dgn-np:NP538466.RAEDzip6anXX06vQYxbvmc2kBlam9n1cBEbwATJ4Bul04130_assertion
dcterms:description
"[The purposes of this study were to examine the TNFR2 polymorphism in Japanese patients with SLE and to investigate its association with other autoimmune diseases accompanied by vasculitis, mixed connective tissue disease, Buerger's disease, and Takayasu's arteritis.]. 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:11169260
;
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:NP538466.RAEDzip6anXX06vQYxbvmc2kBlam9n1cBEbwATJ4Bul04130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}