@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP394231.RAnoPle0alc2w0vc3HOb8Xpt1GsuB3-1vSNxNaI6AFLgU
> .
@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:NP394231.RAnoPle0alc2w0vc3HOb8Xpt1GsuB3-1vSNxNaI6AFLgU130_head
{
this:
np:hasAssertion
dgn-np:NP394231.RAnoPle0alc2w0vc3HOb8Xpt1GsuB3-1vSNxNaI6AFLgU130_assertion
;
np:hasProvenance
dgn-np:NP394231.RAnoPle0alc2w0vc3HOb8Xpt1GsuB3-1vSNxNaI6AFLgU130_provenance
;
np:hasPublicationInfo
dgn-np:NP394231.RAnoPle0alc2w0vc3HOb8Xpt1GsuB3-1vSNxNaI6AFLgU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP394231.RAnoPle0alc2w0vc3HOb8Xpt1GsuB3-1vSNxNaI6AFLgU130_assertion
a
np:Assertion
.
dgn-np:NP394231.RAnoPle0alc2w0vc3HOb8Xpt1GsuB3-1vSNxNaI6AFLgU130_provenance
a
np:Provenance
.
dgn-np:NP394231.RAnoPle0alc2w0vc3HOb8Xpt1GsuB3-1vSNxNaI6AFLgU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP394231.RAnoPle0alc2w0vc3HOb8Xpt1GsuB3-1vSNxNaI6AFLgU130_assertion
{
miriam-gene:1493
a
ncit:C16612
.
lld:C0042900
a
ncit:C7057
.
dgn-gda:DGN9d9d259221924d570a521fd260546492
sio:SIO_000628
miriam-gene:1493
,
lld:C0042900
;
a
sio:SIO_001121
.
}
dgn-np:NP394231.RAnoPle0alc2w0vc3HOb8Xpt1GsuB3-1vSNxNaI6AFLgU130_provenance
{
dgn-np:NP394231.RAnoPle0alc2w0vc3HOb8Xpt1GsuB3-1vSNxNaI6AFLgU130_assertion
dcterms:description
"[Several studies have disclosed an association between the previously known variants of the CTLA4 gene and autoimmune disorders, but no study has as yet found any definite association between vitiligo and the CTLA4 polymorphisms.]. 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:15649153
;
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:NP394231.RAnoPle0alc2w0vc3HOb8Xpt1GsuB3-1vSNxNaI6AFLgU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}