@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP115739.RAEbMzU1JXPvrl-x9TRe9kFLfN5oBw_nq-T36p8bqu3mk
> .
@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:NP115739.RAEbMzU1JXPvrl-x9TRe9kFLfN5oBw_nq-T36p8bqu3mk130_head
{
this:
np:hasAssertion
dgn-np:NP115739.RAEbMzU1JXPvrl-x9TRe9kFLfN5oBw_nq-T36p8bqu3mk130_assertion
;
np:hasProvenance
dgn-np:NP115739.RAEbMzU1JXPvrl-x9TRe9kFLfN5oBw_nq-T36p8bqu3mk130_provenance
;
np:hasPublicationInfo
dgn-np:NP115739.RAEbMzU1JXPvrl-x9TRe9kFLfN5oBw_nq-T36p8bqu3mk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP115739.RAEbMzU1JXPvrl-x9TRe9kFLfN5oBw_nq-T36p8bqu3mk130_assertion
a
np:Assertion
.
dgn-np:NP115739.RAEbMzU1JXPvrl-x9TRe9kFLfN5oBw_nq-T36p8bqu3mk130_provenance
a
np:Provenance
.
dgn-np:NP115739.RAEbMzU1JXPvrl-x9TRe9kFLfN5oBw_nq-T36p8bqu3mk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP115739.RAEbMzU1JXPvrl-x9TRe9kFLfN5oBw_nq-T36p8bqu3mk130_assertion
{
miriam-gene:23495
a
ncit:C16612
.
lld:C0009447
a
ncit:C7057
.
dgn-gda:DGNa4c6b876b9d175e1a376b9717fdc19b5
sio:SIO_000628
miriam-gene:23495
,
lld:C0009447
;
a
sio:SIO_001122
.
}
dgn-np:NP115739.RAEbMzU1JXPvrl-x9TRe9kFLfN5oBw_nq-T36p8bqu3mk130_provenance
{
dgn-np:NP115739.RAEbMzU1JXPvrl-x9TRe9kFLfN5oBw_nq-T36p8bqu3mk130_assertion
dcterms:description
"[This also confirms the previous suggestion that TNFRSF13B defects alone do not cause CVID and that such an extremely heterogeneous immunodeficiency might be more likely related to additional, still unknown environmental and genetic factors.]. 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:19494827
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP115739.RAEbMzU1JXPvrl-x9TRe9kFLfN5oBw_nq-T36p8bqu3mk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:44+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" .
}