@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP424563.RAiIkgngzU6RHXvTvUcyOI1_-R6F7S70guOZ2I9vJ_QPo
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP424563.RAiIkgngzU6RHXvTvUcyOI1_-R6F7S70guOZ2I9vJ_QPo130_head
{
this:
np:hasAssertion
dgn-np:NP424563.RAiIkgngzU6RHXvTvUcyOI1_-R6F7S70guOZ2I9vJ_QPo130_assertion
;
np:hasProvenance
dgn-np:NP424563.RAiIkgngzU6RHXvTvUcyOI1_-R6F7S70guOZ2I9vJ_QPo130_provenance
;
np:hasPublicationInfo
dgn-np:NP424563.RAiIkgngzU6RHXvTvUcyOI1_-R6F7S70guOZ2I9vJ_QPo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP424563.RAiIkgngzU6RHXvTvUcyOI1_-R6F7S70guOZ2I9vJ_QPo130_assertion
a
np:Assertion
.
dgn-np:NP424563.RAiIkgngzU6RHXvTvUcyOI1_-R6F7S70guOZ2I9vJ_QPo130_provenance
a
np:Provenance
.
dgn-np:NP424563.RAiIkgngzU6RHXvTvUcyOI1_-R6F7S70guOZ2I9vJ_QPo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP424563.RAiIkgngzU6RHXvTvUcyOI1_-R6F7S70guOZ2I9vJ_QPo130_assertion
{
miriam-gene:1493
a
ncit:C16612
.
lld:C0018213
a
ncit:C7057
.
dgn-gda:DGN9b3e166c0ec0e9684e8425dccbc1ebba
sio:SIO_000628
miriam-gene:1493
,
lld:C0018213
;
a
sio:SIO_001122
.
}
dgn-np:NP424563.RAiIkgngzU6RHXvTvUcyOI1_-R6F7S70guOZ2I9vJ_QPo130_provenance
{
dgn-np:NP424563.RAiIkgngzU6RHXvTvUcyOI1_-R6F7S70guOZ2I9vJ_QPo130_assertion
dcterms:description
"[Recently, it was shown that, in GD, CT60 (+6230G>A), a single nucleotide polymorphism (SNP) at the end of the CTLA4 transcript, is associated with an alteration in the ratio of splice forms of the CTLA4 gene and that this ratio affects disease susceptibility.]. 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:14675397
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP424563.RAiIkgngzU6RHXvTvUcyOI1_-R6F7S70guOZ2I9vJ_QPo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:57+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}