@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP916659.RAGy13v6eW05atkhS0eJKtwKQTw3-Kmu3kXZH88qeg4dc
> .
@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:NP916659.RAGy13v6eW05atkhS0eJKtwKQTw3-Kmu3kXZH88qeg4dc130_head
{
this:
np:hasAssertion
dgn-np:NP916659.RAGy13v6eW05atkhS0eJKtwKQTw3-Kmu3kXZH88qeg4dc130_assertion
;
np:hasProvenance
dgn-np:NP916659.RAGy13v6eW05atkhS0eJKtwKQTw3-Kmu3kXZH88qeg4dc130_provenance
;
np:hasPublicationInfo
dgn-np:NP916659.RAGy13v6eW05atkhS0eJKtwKQTw3-Kmu3kXZH88qeg4dc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP916659.RAGy13v6eW05atkhS0eJKtwKQTw3-Kmu3kXZH88qeg4dc130_assertion
a
np:Assertion
.
dgn-np:NP916659.RAGy13v6eW05atkhS0eJKtwKQTw3-Kmu3kXZH88qeg4dc130_provenance
a
np:Provenance
.
dgn-np:NP916659.RAGy13v6eW05atkhS0eJKtwKQTw3-Kmu3kXZH88qeg4dc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP916659.RAGy13v6eW05atkhS0eJKtwKQTw3-Kmu3kXZH88qeg4dc130_assertion
{
miriam-gene:7133
a
ncit:C16612
.
lld:C0039263
a
ncit:C7057
.
dgn-gda:DGN4883226c40560301199d78e145f13c02
sio:SIO_000628
miriam-gene:7133
,
lld:C0039263
;
a
sio:SIO_001121
.
}
dgn-np:NP916659.RAGy13v6eW05atkhS0eJKtwKQTw3-Kmu3kXZH88qeg4dc130_provenance
{
dgn-np:NP916659.RAGy13v6eW05atkhS0eJKtwKQTw3-Kmu3kXZH88qeg4dc130_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:NP916659.RAGy13v6eW05atkhS0eJKtwKQTw3-Kmu3kXZH88qeg4dc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:22+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" .
}