@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g
> .
@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:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_head
{
this:
np:hasAssertion
dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_assertion
;
np:hasProvenance
dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_provenance
;
np:hasPublicationInfo
dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_assertion
a
np:Assertion
.
dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_provenance
a
np:Provenance
.
dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_assertion
{
miriam-gene:11197
a
ncit:C16612
.
lld:C0025218
a
ncit:C7057
.
dgn-gda:DGN0bae914cc27efc6d63af5ece37249a6c
sio:SIO_000628
miriam-gene:11197
,
lld:C0025218
;
a
sio:SIO_001121
.
}
dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_provenance
{
dgn-np:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_assertion
dcterms:description
"[Collectively, WIF-1 downregulation, which may occur in epidermal keratinocytes and in dermal fibroblasts, is involved in melasma development because of the stimulation of melanogenesis and melanosome transfer through upregulation of the canonical and the noncanonical Wnt signaling pathway.]. 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:22951732
;
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:NP660348.RA7tOA4Aro8bMxLxd3XzVs5JHQgph0Gftd2DM9xFJXL1g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:39+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" .
}