@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP379910.RABDvXj-rOMFvzRvc9nHSMEj2t4Ai6pG6lDbIiEew4WcA
> .
@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 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:NP379910.RABDvXj-rOMFvzRvc9nHSMEj2t4Ai6pG6lDbIiEew4WcA130_head
{
this:
np:hasAssertion
dgn-np:NP379910.RABDvXj-rOMFvzRvc9nHSMEj2t4Ai6pG6lDbIiEew4WcA130_assertion
;
np:hasProvenance
dgn-np:NP379910.RABDvXj-rOMFvzRvc9nHSMEj2t4Ai6pG6lDbIiEew4WcA130_provenance
;
np:hasPublicationInfo
dgn-np:NP379910.RABDvXj-rOMFvzRvc9nHSMEj2t4Ai6pG6lDbIiEew4WcA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP379910.RABDvXj-rOMFvzRvc9nHSMEj2t4Ai6pG6lDbIiEew4WcA130_assertion
a
np:Assertion
.
dgn-np:NP379910.RABDvXj-rOMFvzRvc9nHSMEj2t4Ai6pG6lDbIiEew4WcA130_provenance
a
np:Provenance
.
dgn-np:NP379910.RABDvXj-rOMFvzRvc9nHSMEj2t4Ai6pG6lDbIiEew4WcA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP379910.RABDvXj-rOMFvzRvc9nHSMEj2t4Ai6pG6lDbIiEew4WcA130_assertion
{
miriam-gene:8013
a
ncit:C16612
.
lld:C1801959
a
ncit:C7057
.
dgn-gda:DGN3d4d5844c65dfc22d33ea5144f9a0eec
sio:SIO_000628
miriam-gene:8013
,
lld:C1801959
;
a
sio:SIO_001121
.
}
dgn-np:NP379910.RABDvXj-rOMFvzRvc9nHSMEj2t4Ai6pG6lDbIiEew4WcA130_provenance
{
dgn-np:NP379910.RABDvXj-rOMFvzRvc9nHSMEj2t4Ai6pG6lDbIiEew4WcA130_assertion
dc:description
"[Our data provide evidence that severe defects of thymopoiesis impinge on TEC homeostasis and may affect deletional and nondeletional mechanisms of central tolerance, thus favoring immune dysreactive manifestations, as in Omenn syndrome.]. 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:19414857
;
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:NP379910.RABDvXj-rOMFvzRvc9nHSMEj2t4Ai6pG6lDbIiEew4WcA130_publicationInfo
{
this:
dc:created
"2014-10-02T12:35:44+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}