@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP873898.RAmtVo62DahH7upkdnbebDsDOc-gmds1ePv-NDsqUb7WA
> .
@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/v3.0.0/void/
> .
dgn-np:NP873898.RAmtVo62DahH7upkdnbebDsDOc-gmds1ePv-NDsqUb7WA130_head
{
this:
np:hasAssertion
dgn-np:NP873898.RAmtVo62DahH7upkdnbebDsDOc-gmds1ePv-NDsqUb7WA130_assertion
;
np:hasProvenance
dgn-np:NP873898.RAmtVo62DahH7upkdnbebDsDOc-gmds1ePv-NDsqUb7WA130_provenance
;
np:hasPublicationInfo
dgn-np:NP873898.RAmtVo62DahH7upkdnbebDsDOc-gmds1ePv-NDsqUb7WA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP873898.RAmtVo62DahH7upkdnbebDsDOc-gmds1ePv-NDsqUb7WA130_assertion
a
np:Assertion
.
dgn-np:NP873898.RAmtVo62DahH7upkdnbebDsDOc-gmds1ePv-NDsqUb7WA130_provenance
a
np:Provenance
.
dgn-np:NP873898.RAmtVo62DahH7upkdnbebDsDOc-gmds1ePv-NDsqUb7WA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP873898.RAmtVo62DahH7upkdnbebDsDOc-gmds1ePv-NDsqUb7WA130_assertion
{
miriam-gene:23495
a
ncit:C16612
.
lld:C0009447
a
ncit:C7057
.
dgn-gda:DGNd25bdf8585e222f49f5931ce21db8676
sio:SIO_000628
miriam-gene:23495
,
lld:C0009447
;
a
sio:SIO_001121
.
}
dgn-np:NP873898.RAmtVo62DahH7upkdnbebDsDOc-gmds1ePv-NDsqUb7WA130_provenance
{
dgn-np:NP873898.RAmtVo62DahH7upkdnbebDsDOc-gmds1ePv-NDsqUb7WA130_assertion
dcterms:description
"[Heterozygous deleterious mutations in the gene encoding the tumor necrosis factor receptor superfamily member 13b (TNFRSF13B), or transmembrane activator and CAML interactor (TACI), have been associated with the development of common variable immunodeficiency.]. 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:21514638
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP873898.RAmtVo62DahH7upkdnbebDsDOc-gmds1ePv-NDsqUb7WA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:32+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}