@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP607748.RAuI857zMJQD3IN6ZGDiKFEmtmWEavdARXD7rv5MK6RBU
> .
@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:NP607748.RAuI857zMJQD3IN6ZGDiKFEmtmWEavdARXD7rv5MK6RBU130_head
{
this:
np:hasAssertion
dgn-np:NP607748.RAuI857zMJQD3IN6ZGDiKFEmtmWEavdARXD7rv5MK6RBU130_assertion
;
np:hasProvenance
dgn-np:NP607748.RAuI857zMJQD3IN6ZGDiKFEmtmWEavdARXD7rv5MK6RBU130_provenance
;
np:hasPublicationInfo
dgn-np:NP607748.RAuI857zMJQD3IN6ZGDiKFEmtmWEavdARXD7rv5MK6RBU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP607748.RAuI857zMJQD3IN6ZGDiKFEmtmWEavdARXD7rv5MK6RBU130_assertion
a
np:Assertion
.
dgn-np:NP607748.RAuI857zMJQD3IN6ZGDiKFEmtmWEavdARXD7rv5MK6RBU130_provenance
a
np:Provenance
.
dgn-np:NP607748.RAuI857zMJQD3IN6ZGDiKFEmtmWEavdARXD7rv5MK6RBU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP607748.RAuI857zMJQD3IN6ZGDiKFEmtmWEavdARXD7rv5MK6RBU130_assertion
{
miriam-gene:23495
a
ncit:C16612
.
lld:C0086438
a
ncit:C7057
.
dgn-gda:DGN732319e55d998a66a7c49907c5a49f00
sio:SIO_000628
miriam-gene:23495
,
lld:C0086438
;
a
sio:SIO_001121
.
}
dgn-np:NP607748.RAuI857zMJQD3IN6ZGDiKFEmtmWEavdARXD7rv5MK6RBU130_provenance
{
dgn-np:NP607748.RAuI857zMJQD3IN6ZGDiKFEmtmWEavdARXD7rv5MK6RBU130_assertion
dcterms:description
"[The genetic complexity and variable clinical presentation of TACI deficiency prompted us to evaluate the genetic, immunologic, and clinical condition in 50 individuals with TNFRSF13B alterations, following screening of 564 unrelated patients with hypogammaglobulinemia.]. 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:18981294
;
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:NP607748.RAuI857zMJQD3IN6ZGDiKFEmtmWEavdARXD7rv5MK6RBU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:04+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" .
}