@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk
> .
@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:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_head
{
this:
np:hasAssertion
dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_assertion
;
np:hasProvenance
dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_provenance
;
np:hasPublicationInfo
dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_assertion
a
np:Assertion
.
dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_provenance
a
np:Provenance
.
dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_assertion
{
miriam-gene:871
a
ncit:C16612
.
lld:C0022548
a
ncit:C7057
.
dgn-gda:DGNd27e3a3450027a4c98f4638f33086ca8
sio:SIO_000628
miriam-gene:871
,
lld:C0022548
;
a
sio:SIO_001121
.
}
dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_provenance
{
dgn-np:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_assertion
dcterms:description
"[Combining the results of our previous in vitro experiment results, we suggest that overexpression of HSP47 in keloid fibroblast cells could induce excessive collagen accumulation by enhancing collagen synthesis, which not only presents a possible mechanism of keloid formation, but also offers a therapeutic potential of RNA interference to HSP47 for the treatment of keloids and other fibroproliferative disorders.]. 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:22295344
;
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:NP161178.RARSh1tvi-LAWIuiwMCUQ1Vg03iRH8_JaS0VwLdUDNzVk130_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" .
}