@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP382669.RARYjG30ppFxexgtQ-MXRf88g03S-4oNHBQblDC7alYWA
> .
@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:NP382669.RARYjG30ppFxexgtQ-MXRf88g03S-4oNHBQblDC7alYWA130_head
{
this:
np:hasAssertion
dgn-np:NP382669.RARYjG30ppFxexgtQ-MXRf88g03S-4oNHBQblDC7alYWA130_assertion
;
np:hasProvenance
dgn-np:NP382669.RARYjG30ppFxexgtQ-MXRf88g03S-4oNHBQblDC7alYWA130_provenance
;
np:hasPublicationInfo
dgn-np:NP382669.RARYjG30ppFxexgtQ-MXRf88g03S-4oNHBQblDC7alYWA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP382669.RARYjG30ppFxexgtQ-MXRf88g03S-4oNHBQblDC7alYWA130_assertion
a
np:Assertion
.
dgn-np:NP382669.RARYjG30ppFxexgtQ-MXRf88g03S-4oNHBQblDC7alYWA130_provenance
a
np:Provenance
.
dgn-np:NP382669.RARYjG30ppFxexgtQ-MXRf88g03S-4oNHBQblDC7alYWA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP382669.RARYjG30ppFxexgtQ-MXRf88g03S-4oNHBQblDC7alYWA130_assertion
{
miriam-gene:1734
a
ncit:C16612
.
lld:C1849718
a
ncit:C7057
.
dgn-gda:DGN54c92060fb5830941a09baf15748988d
sio:SIO_000628
miriam-gene:1734
,
lld:C1849718
;
a
sio:SIO_001121
.
}
dgn-np:NP382669.RARYjG30ppFxexgtQ-MXRf88g03S-4oNHBQblDC7alYWA130_provenance
{
dgn-np:NP382669.RARYjG30ppFxexgtQ-MXRf88g03S-4oNHBQblDC7alYWA130_assertion
dcterms:description
"[These results suggest that D2 expression is increased by BPS and suppressed by PDGF in hCASMCs, and that intracellular thyroid hormone activation may be involved in the suppression of DNA synthesis and migration activity of hCASMCs.]. 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:16140305
;
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:NP382669.RARYjG30ppFxexgtQ-MXRf88g03S-4oNHBQblDC7alYWA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:46+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" .
}