@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU
> .
@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:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_head
{
this:
np:hasAssertion
dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_assertion
;
np:hasProvenance
dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_provenance
;
np:hasPublicationInfo
dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_assertion
a
np:Assertion
.
dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_provenance
a
np:Provenance
.
dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_assertion
{
miriam-gene:1490
a
ncit:C16612
.
lld:C0036421
a
ncit:C7057
.
dgn-gda:DGN2e00217a1ef1522e65e02cc1f881334d
sio:SIO_000628
miriam-gene:1490
,
lld:C0036421
;
a
sio:SIO_001121
.
}
dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_provenance
{
dgn-np:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_assertion
dcterms:description
"[These data indicate that there is an overexpression of CTGF in the systemic sclerosis cells, probably due to increased gene transcription, and suggest that the dysregulation of CTGF production is an important factor in fibroblast activation and the excessive deposition of collagen in systemic sclerosis.]. 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:10942593
;
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:NP160903.RAp_gkMXsXKMYbpSiiXTh5KFQe81hsybc_dPvirlxoKfU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:27+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" .
}