@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP784239.RADoADhmotVkN55_0rldHLwxgsC-6t7GQyUCWsPZg1LIQ
> .
@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:NP784239.RADoADhmotVkN55_0rldHLwxgsC-6t7GQyUCWsPZg1LIQ130_head
{
this:
np:hasAssertion
dgn-np:NP784239.RADoADhmotVkN55_0rldHLwxgsC-6t7GQyUCWsPZg1LIQ130_assertion
;
np:hasProvenance
dgn-np:NP784239.RADoADhmotVkN55_0rldHLwxgsC-6t7GQyUCWsPZg1LIQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP784239.RADoADhmotVkN55_0rldHLwxgsC-6t7GQyUCWsPZg1LIQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP784239.RADoADhmotVkN55_0rldHLwxgsC-6t7GQyUCWsPZg1LIQ130_assertion
a
np:Assertion
.
dgn-np:NP784239.RADoADhmotVkN55_0rldHLwxgsC-6t7GQyUCWsPZg1LIQ130_provenance
a
np:Provenance
.
dgn-np:NP784239.RADoADhmotVkN55_0rldHLwxgsC-6t7GQyUCWsPZg1LIQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP784239.RADoADhmotVkN55_0rldHLwxgsC-6t7GQyUCWsPZg1LIQ130_assertion
{
miriam-gene:2113
a
ncit:C16612
.
lld:C0003864
a
ncit:C7057
.
dgn-gda:DGNef86ec40f8630cf43354f66c4e20c24a
sio:SIO_000628
miriam-gene:2113
,
lld:C0003864
;
a
sio:SIO_001121
.
}
dgn-np:NP784239.RADoADhmotVkN55_0rldHLwxgsC-6t7GQyUCWsPZg1LIQ130_provenance
{
dgn-np:NP784239.RADoADhmotVkN55_0rldHLwxgsC-6t7GQyUCWsPZg1LIQ130_assertion
dcterms:description
"[Through stratified analysis, TNFAIP3 and ETS1 showed significant associations with multiple SLE subphenotypes (such as malar rash, arthritis, hematologic disorder and antinuclear antibody) while TNIP1 just showed relatively weak association with onset age.]. 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:22087647
;
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:NP784239.RADoADhmotVkN55_0rldHLwxgsC-6t7GQyUCWsPZg1LIQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:55+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" .
}