@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP807642.RAOlv1LTjURcQUhLI3PA8hHAHtd5Xzbpqnb3dbnAG5Wqw
> .
@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:NP807642.RAOlv1LTjURcQUhLI3PA8hHAHtd5Xzbpqnb3dbnAG5Wqw130_head
{
this:
np:hasAssertion
dgn-np:NP807642.RAOlv1LTjURcQUhLI3PA8hHAHtd5Xzbpqnb3dbnAG5Wqw130_assertion
;
np:hasProvenance
dgn-np:NP807642.RAOlv1LTjURcQUhLI3PA8hHAHtd5Xzbpqnb3dbnAG5Wqw130_provenance
;
np:hasPublicationInfo
dgn-np:NP807642.RAOlv1LTjURcQUhLI3PA8hHAHtd5Xzbpqnb3dbnAG5Wqw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP807642.RAOlv1LTjURcQUhLI3PA8hHAHtd5Xzbpqnb3dbnAG5Wqw130_assertion
a
np:Assertion
.
dgn-np:NP807642.RAOlv1LTjURcQUhLI3PA8hHAHtd5Xzbpqnb3dbnAG5Wqw130_provenance
a
np:Provenance
.
dgn-np:NP807642.RAOlv1LTjURcQUhLI3PA8hHAHtd5Xzbpqnb3dbnAG5Wqw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP807642.RAOlv1LTjURcQUhLI3PA8hHAHtd5Xzbpqnb3dbnAG5Wqw130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0175697
a
ncit:C7057
.
dgn-gda:DGN0e2d68e091601a6baa90c8310f580f8b
sio:SIO_000628
miriam-gene:64127
,
lld:C0175697
;
a
sio:SIO_001121
.
}
dgn-np:NP807642.RAOlv1LTjURcQUhLI3PA8hHAHtd5Xzbpqnb3dbnAG5Wqw130_provenance
{
dgn-np:NP807642.RAOlv1LTjURcQUhLI3PA8hHAHtd5Xzbpqnb3dbnAG5Wqw130_assertion
dc:description
"[This was reproduced at the gene level with rapid induction (<4 h) and, unlike for LPS stimulation, was still sustained at 24 h. Using transfected and native muramyl dipeptide (MDP), which is a cleavage product of PGN and a specific NOD2 agonist, in assays with wild type cells or those from patients with Crohn's disease carrying the Leu1007 frameshift mutation of NOD2, we showed that (i) both NOD2 dependent and independent signalling (appearing TLR2 mediated) occurred for PGN upregulation of PD-L1 (ii) upregulation is lost in response to MDP in patients with the homozygous mutation and (iii) PD-L1 upregulation was unaffected in patients with heterozygous mutations as previously reported for cytokine responses to MDP.]. 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:22397822
;
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:NP807642.RAOlv1LTjURcQUhLI3PA8hHAHtd5Xzbpqnb3dbnAG5Wqw130_publicationInfo
{
this:
dc:created
"2014-10-02T12:40:15+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
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}