@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP698661.RADP7jU6qdNNTMA5MWtp44Ygbz2A3ZvwgDN-MEBhP-iws
> .
@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:NP698661.RADP7jU6qdNNTMA5MWtp44Ygbz2A3ZvwgDN-MEBhP-iws130_head
{
this:
np:hasAssertion
dgn-np:NP698661.RADP7jU6qdNNTMA5MWtp44Ygbz2A3ZvwgDN-MEBhP-iws130_assertion
;
np:hasProvenance
dgn-np:NP698661.RADP7jU6qdNNTMA5MWtp44Ygbz2A3ZvwgDN-MEBhP-iws130_provenance
;
np:hasPublicationInfo
dgn-np:NP698661.RADP7jU6qdNNTMA5MWtp44Ygbz2A3ZvwgDN-MEBhP-iws130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP698661.RADP7jU6qdNNTMA5MWtp44Ygbz2A3ZvwgDN-MEBhP-iws130_assertion
a
np:Assertion
.
dgn-np:NP698661.RADP7jU6qdNNTMA5MWtp44Ygbz2A3ZvwgDN-MEBhP-iws130_provenance
a
np:Provenance
.
dgn-np:NP698661.RADP7jU6qdNNTMA5MWtp44Ygbz2A3ZvwgDN-MEBhP-iws130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP698661.RADP7jU6qdNNTMA5MWtp44Ygbz2A3ZvwgDN-MEBhP-iws130_assertion
{
miriam-gene:348120
a
ncit:C16612
.
lld:C0178468
a
ncit:C7057
.
dgn-gda:DGN5299fd17dc590befcada6ae4589a211e
sio:SIO_000628
miriam-gene:348120
,
lld:C0178468
;
a
sio:SIO_001121
.
}
dgn-np:NP698661.RADP7jU6qdNNTMA5MWtp44Ygbz2A3ZvwgDN-MEBhP-iws130_provenance
{
dgn-np:NP698661.RADP7jU6qdNNTMA5MWtp44Ygbz2A3ZvwgDN-MEBhP-iws130_assertion
dcterms:description
"[Our data show a significant effect of the CTLA4 CT60G allele at the homozygous state on the risk of developing AITD in children with CD and suggest that the reported association of the CTLA4 CT60 A/G polymorphism with CD is limited to the subgroup of patients who are or will be complicated with AITD.]. 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:18929517
;
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:NP698661.RADP7jU6qdNNTMA5MWtp44Ygbz2A3ZvwgDN-MEBhP-iws130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:01+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" .
}