@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP696488.RA3hyGL_j2MhbXDF1nRcyPNlJ9Z21p2lq3odJNEaRzwqA
> .
@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:NP696488.RA3hyGL_j2MhbXDF1nRcyPNlJ9Z21p2lq3odJNEaRzwqA130_head
{
this:
np:hasAssertion
dgn-np:NP696488.RA3hyGL_j2MhbXDF1nRcyPNlJ9Z21p2lq3odJNEaRzwqA130_assertion
;
np:hasProvenance
dgn-np:NP696488.RA3hyGL_j2MhbXDF1nRcyPNlJ9Z21p2lq3odJNEaRzwqA130_provenance
;
np:hasPublicationInfo
dgn-np:NP696488.RA3hyGL_j2MhbXDF1nRcyPNlJ9Z21p2lq3odJNEaRzwqA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP696488.RA3hyGL_j2MhbXDF1nRcyPNlJ9Z21p2lq3odJNEaRzwqA130_assertion
a
np:Assertion
.
dgn-np:NP696488.RA3hyGL_j2MhbXDF1nRcyPNlJ9Z21p2lq3odJNEaRzwqA130_provenance
a
np:Provenance
.
dgn-np:NP696488.RA3hyGL_j2MhbXDF1nRcyPNlJ9Z21p2lq3odJNEaRzwqA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP696488.RA3hyGL_j2MhbXDF1nRcyPNlJ9Z21p2lq3odJNEaRzwqA130_assertion
{
miriam-gene:7965
a
ncit:C16612
.
lld:C0029408
a
ncit:C7057
.
dgn-gda:DGN4842b3f6f19826086e7004114235ca78
sio:SIO_000628
miriam-gene:7965
,
lld:C0029408
;
a
sio:SIO_001121
.
}
dgn-np:NP696488.RA3hyGL_j2MhbXDF1nRcyPNlJ9Z21p2lq3odJNEaRzwqA130_provenance
{
dgn-np:NP696488.RA3hyGL_j2MhbXDF1nRcyPNlJ9Z21p2lq3odJNEaRzwqA130_assertion
dcterms:description
"[We conclude that transamidation by TG2 transforms S100A11 into a covalently bonded homodimer that acquires the capacity to signal through the p38 MAPK pathway, accelerate chondrocyte hypertrophy and matrix catabolism, and thereby couple inflammation with chondrocyte activation to potentially promote OA progression.]. 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:18523305
;
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:NP696488.RA3hyGL_j2MhbXDF1nRcyPNlJ9Z21p2lq3odJNEaRzwqA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:03+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" .
}