@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP431439.RARg0BVsIo4oiTv8NERj2Zt0DgoM8kcmi3hMm5jrEKlj8
> .
@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:NP431439.RARg0BVsIo4oiTv8NERj2Zt0DgoM8kcmi3hMm5jrEKlj8130_head
{
this:
np:hasAssertion
dgn-np:NP431439.RARg0BVsIo4oiTv8NERj2Zt0DgoM8kcmi3hMm5jrEKlj8130_assertion
;
np:hasProvenance
dgn-np:NP431439.RARg0BVsIo4oiTv8NERj2Zt0DgoM8kcmi3hMm5jrEKlj8130_provenance
;
np:hasPublicationInfo
dgn-np:NP431439.RARg0BVsIo4oiTv8NERj2Zt0DgoM8kcmi3hMm5jrEKlj8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP431439.RARg0BVsIo4oiTv8NERj2Zt0DgoM8kcmi3hMm5jrEKlj8130_assertion
a
np:Assertion
.
dgn-np:NP431439.RARg0BVsIo4oiTv8NERj2Zt0DgoM8kcmi3hMm5jrEKlj8130_provenance
a
np:Provenance
.
dgn-np:NP431439.RARg0BVsIo4oiTv8NERj2Zt0DgoM8kcmi3hMm5jrEKlj8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP431439.RARg0BVsIo4oiTv8NERj2Zt0DgoM8kcmi3hMm5jrEKlj8130_assertion
{
miriam-gene:6422
a
ncit:C16612
.
lld:C0409959
a
ncit:C7057
.
dgn-gda:DGN4d30c00cf43b8bdd67cc39a6faa37964
sio:SIO_000628
miriam-gene:6422
,
lld:C0409959
;
a
sio:SIO_001121
.
}
dgn-np:NP431439.RARg0BVsIo4oiTv8NERj2Zt0DgoM8kcmi3hMm5jrEKlj8130_provenance
{
dgn-np:NP431439.RARg0BVsIo4oiTv8NERj2Zt0DgoM8kcmi3hMm5jrEKlj8130_assertion
dcterms:description
"[Given the role of Wnt signalling during chondrogenesis and in maintaining the integrity of the long lived articular chondrocytes, we conclude from our results that the reduced Sfrp1 expression in STR/ort mice not only leads to an increased activation of the Wnt/β-catenin signalling early in life but also renders the articular cartilage prone to premature ageing and to the development of OA.]. 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:23261541
;
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:NP431439.RARg0BVsIo4oiTv8NERj2Zt0DgoM8kcmi3hMm5jrEKlj8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:15+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" .
}