@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A
> .
@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:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_head
{
this:
np:hasAssertion
dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_assertion
;
np:hasProvenance
dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_provenance
;
np:hasPublicationInfo
dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_assertion
a
np:Assertion
.
dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_provenance
a
np:Provenance
.
dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_assertion
{
miriam-gene:3595
a
ncit:C16612
.
lld:C0023348
a
ncit:C7057
.
dgn-gda:DGN5a5e667a00a68f135ca35ee343922267
sio:SIO_000628
miriam-gene:3595
,
lld:C0023348
;
a
sio:SIO_001121
.
}
dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_provenance
{
dgn-np:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_assertion
dcterms:description
"[Single nucleotide polymorphisms (SNPs) in the 5' flanking region of IL12RB2 are frequently detected in lepromatous leprosy patients, and may be possible immunogenetic factors that reduce transcriptional activity of the IL-12Rbeta2 gene in Jurkat T cells.]. 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:18771340
;
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:NP507337.RAtpqyfDuCw5zP51wEzuZ5NZ-GjU8hX-4m6IGfMJbnH4A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:02+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" .
}