@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP653192.RA-BGwyYVmTbQG1GUGyLyfanVLPn2WpqdeSLv9TDC9TgA
> .
@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:NP653192.RA-BGwyYVmTbQG1GUGyLyfanVLPn2WpqdeSLv9TDC9TgA130_head
{
this:
np:hasAssertion
dgn-np:NP653192.RA-BGwyYVmTbQG1GUGyLyfanVLPn2WpqdeSLv9TDC9TgA130_assertion
;
np:hasProvenance
dgn-np:NP653192.RA-BGwyYVmTbQG1GUGyLyfanVLPn2WpqdeSLv9TDC9TgA130_provenance
;
np:hasPublicationInfo
dgn-np:NP653192.RA-BGwyYVmTbQG1GUGyLyfanVLPn2WpqdeSLv9TDC9TgA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP653192.RA-BGwyYVmTbQG1GUGyLyfanVLPn2WpqdeSLv9TDC9TgA130_assertion
a
np:Assertion
.
dgn-np:NP653192.RA-BGwyYVmTbQG1GUGyLyfanVLPn2WpqdeSLv9TDC9TgA130_provenance
a
np:Provenance
.
dgn-np:NP653192.RA-BGwyYVmTbQG1GUGyLyfanVLPn2WpqdeSLv9TDC9TgA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP653192.RA-BGwyYVmTbQG1GUGyLyfanVLPn2WpqdeSLv9TDC9TgA130_assertion
{
miriam-gene:6667
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN966a1570569cbc7510284c5c756c2e49
sio:SIO_000628
miriam-gene:6667
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP653192.RA-BGwyYVmTbQG1GUGyLyfanVLPn2WpqdeSLv9TDC9TgA130_provenance
{
dgn-np:NP653192.RA-BGwyYVmTbQG1GUGyLyfanVLPn2WpqdeSLv9TDC9TgA130_assertion
dcterms:description
"[Although DNA copy number loss is responsible for downregulation of phosphatidylinositol 4,5-bisphosphate 5-phosphatase in a proportion of melanomas, histone hypoacetylation mediated by histone deacetylases HDAC2 and HDAC3 through binding to the transcription factor Sp1 at the PIB5PA gene promoter appears to be another commonly involved mechanism.]. 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:23443536
;
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:NP653192.RA-BGwyYVmTbQG1GUGyLyfanVLPn2WpqdeSLv9TDC9TgA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:33+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" .
}