@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP315764.RARtVAUF0QJ1tb8va3UAOrYmn-Tz4zI6PMzb69GV0WU14
> .
@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:NP315764.RARtVAUF0QJ1tb8va3UAOrYmn-Tz4zI6PMzb69GV0WU14130_head
{
this:
np:hasAssertion
dgn-np:NP315764.RARtVAUF0QJ1tb8va3UAOrYmn-Tz4zI6PMzb69GV0WU14130_assertion
;
np:hasProvenance
dgn-np:NP315764.RARtVAUF0QJ1tb8va3UAOrYmn-Tz4zI6PMzb69GV0WU14130_provenance
;
np:hasPublicationInfo
dgn-np:NP315764.RARtVAUF0QJ1tb8va3UAOrYmn-Tz4zI6PMzb69GV0WU14130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315764.RARtVAUF0QJ1tb8va3UAOrYmn-Tz4zI6PMzb69GV0WU14130_assertion
a
np:Assertion
.
dgn-np:NP315764.RARtVAUF0QJ1tb8va3UAOrYmn-Tz4zI6PMzb69GV0WU14130_provenance
a
np:Provenance
.
dgn-np:NP315764.RARtVAUF0QJ1tb8va3UAOrYmn-Tz4zI6PMzb69GV0WU14130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315764.RARtVAUF0QJ1tb8va3UAOrYmn-Tz4zI6PMzb69GV0WU14130_assertion
{
miriam-gene:7494
a
ncit:C16612
.
lld:C0021390
a
ncit:C7057
.
dgn-gda:DGNb76e0f4d52265d9f13fefd85348eea23
sio:SIO_000628
miriam-gene:7494
,
lld:C0021390
;
a
sio:SIO_001121
.
}
dgn-np:NP315764.RARtVAUF0QJ1tb8va3UAOrYmn-Tz4zI6PMzb69GV0WU14130_provenance
{
dgn-np:NP315764.RARtVAUF0QJ1tb8va3UAOrYmn-Tz4zI6PMzb69GV0WU14130_assertion
dcterms:description
"[We report that Xbp1 deletion in intestinal epithelial cells (IECs) results in spontaneous enteritis and increased susceptibility to induced colitis secondary to both Paneth cell dysfunction and an epithelium that is overly reactive to inducers of IBD such as bacterial products (flagellin) and TNFalpha.]. 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:18775308
;
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:NP315764.RARtVAUF0QJ1tb8va3UAOrYmn-Tz4zI6PMzb69GV0WU14130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:01+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" .
}