@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y
> .
@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:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_head
{
this:
np:hasAssertion
dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_assertion
;
np:hasProvenance
dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_assertion
a
np:Assertion
.
dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_provenance
a
np:Provenance
.
dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_assertion
{
miriam-gene:23495
a
ncit:C16612
.
lld:C0272238
a
ncit:C7057
.
dgn-gda:DGNe02e864859b55a84f7ef9f14d0865cdf
sio:SIO_000628
miriam-gene:23495
,
lld:C0272238
;
a
sio:SIO_001121
.
}
dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_provenance
{
dgn-np:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_assertion
dcterms:description
"[Considering that TNFRSF13B/TACI is very polymorphic and the frequency of its alterations may be different in various ethnic groups, we analyzed their prevalence in 47 Greek patients with antibody deficiencies, including CVID (16 patients), IgAD (16 patients), selective IgG4D (11 patients), and transient hypogammaglobulinemia of infancy (4 patients).]. 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:21547394
;
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:NP585788.RAevMsOrwkukcmTF_CMd4harB9K3FRftMOMoGwKVr_l_Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:52+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
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pav:authoredBy
<
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> , <
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" .
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"v2.1.0" .
}