@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP857758.RAyKvI7zAdsrnRbQvZyZdDQW9wiC9xYWWeaHcQuny4NYI
> .
@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:NP857758.RAyKvI7zAdsrnRbQvZyZdDQW9wiC9xYWWeaHcQuny4NYI130_head
{
this:
np:hasAssertion
dgn-np:NP857758.RAyKvI7zAdsrnRbQvZyZdDQW9wiC9xYWWeaHcQuny4NYI130_assertion
;
np:hasProvenance
dgn-np:NP857758.RAyKvI7zAdsrnRbQvZyZdDQW9wiC9xYWWeaHcQuny4NYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP857758.RAyKvI7zAdsrnRbQvZyZdDQW9wiC9xYWWeaHcQuny4NYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP857758.RAyKvI7zAdsrnRbQvZyZdDQW9wiC9xYWWeaHcQuny4NYI130_assertion
a
np:Assertion
.
dgn-np:NP857758.RAyKvI7zAdsrnRbQvZyZdDQW9wiC9xYWWeaHcQuny4NYI130_provenance
a
np:Provenance
.
dgn-np:NP857758.RAyKvI7zAdsrnRbQvZyZdDQW9wiC9xYWWeaHcQuny4NYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP857758.RAyKvI7zAdsrnRbQvZyZdDQW9wiC9xYWWeaHcQuny4NYI130_assertion
{
miriam-gene:7441
a
ncit:C16612
.
lld:C0021053
a
ncit:C7057
.
dgn-gda:DGN5784272472d81cc7e75471ded1212198
sio:SIO_000628
miriam-gene:7441
,
lld:C0021053
;
a
sio:SIO_001121
.
}
dgn-np:NP857758.RAyKvI7zAdsrnRbQvZyZdDQW9wiC9xYWWeaHcQuny4NYI130_provenance
{
dgn-np:NP857758.RAyKvI7zAdsrnRbQvZyZdDQW9wiC9xYWWeaHcQuny4NYI130_assertion
dcterms:description
"[In humans, a copy number loss of 22q11.2, a region harboring the VPREB1 gene, has been suggested to be associated with several immunologic disorders, but there has been no study on the copy number variation (CNV) of the VPREB1 and its potential association with RA.]. 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:21144590
;
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:NP857758.RAyKvI7zAdsrnRbQvZyZdDQW9wiC9xYWWeaHcQuny4NYI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:13+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" .
}