@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP446362.RAWrlTGF3QK29ldQgI9SVmEaoATyYEu4P_IsO3tqy36Bw
> .
@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:NP446362.RAWrlTGF3QK29ldQgI9SVmEaoATyYEu4P_IsO3tqy36Bw130_head
{
this:
np:hasAssertion
dgn-np:NP446362.RAWrlTGF3QK29ldQgI9SVmEaoATyYEu4P_IsO3tqy36Bw130_assertion
;
np:hasProvenance
dgn-np:NP446362.RAWrlTGF3QK29ldQgI9SVmEaoATyYEu4P_IsO3tqy36Bw130_provenance
;
np:hasPublicationInfo
dgn-np:NP446362.RAWrlTGF3QK29ldQgI9SVmEaoATyYEu4P_IsO3tqy36Bw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP446362.RAWrlTGF3QK29ldQgI9SVmEaoATyYEu4P_IsO3tqy36Bw130_assertion
a
np:Assertion
.
dgn-np:NP446362.RAWrlTGF3QK29ldQgI9SVmEaoATyYEu4P_IsO3tqy36Bw130_provenance
a
np:Provenance
.
dgn-np:NP446362.RAWrlTGF3QK29ldQgI9SVmEaoATyYEu4P_IsO3tqy36Bw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP446362.RAWrlTGF3QK29ldQgI9SVmEaoATyYEu4P_IsO3tqy36Bw130_assertion
{
miriam-gene:7149
a
ncit:C16612
.
lld:C1801959
a
ncit:C7057
.
dgn-gda:DGN6e8450403681c91ccdaa6c417f65b94a
sio:SIO_000628
miriam-gene:7149
,
lld:C1801959
;
a
sio:SIO_001121
.
}
dgn-np:NP446362.RAWrlTGF3QK29ldQgI9SVmEaoATyYEu4P_IsO3tqy36Bw130_provenance
{
dgn-np:NP446362.RAWrlTGF3QK29ldQgI9SVmEaoATyYEu4P_IsO3tqy36Bw130_assertion
dcterms: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:NP446362.RAWrlTGF3QK29ldQgI9SVmEaoATyYEu4P_IsO3tqy36Bw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:26+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" .
}