@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP558094.RANskCjcNoqnI7OFuVA3AvEA_i_6--m2L720b7t48QUQM
> .
@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:NP558094.RANskCjcNoqnI7OFuVA3AvEA_i_6--m2L720b7t48QUQM130_head
{
this:
np:hasAssertion
dgn-np:NP558094.RANskCjcNoqnI7OFuVA3AvEA_i_6--m2L720b7t48QUQM130_assertion
;
np:hasProvenance
dgn-np:NP558094.RANskCjcNoqnI7OFuVA3AvEA_i_6--m2L720b7t48QUQM130_provenance
;
np:hasPublicationInfo
dgn-np:NP558094.RANskCjcNoqnI7OFuVA3AvEA_i_6--m2L720b7t48QUQM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP558094.RANskCjcNoqnI7OFuVA3AvEA_i_6--m2L720b7t48QUQM130_assertion
a
np:Assertion
.
dgn-np:NP558094.RANskCjcNoqnI7OFuVA3AvEA_i_6--m2L720b7t48QUQM130_provenance
a
np:Provenance
.
dgn-np:NP558094.RANskCjcNoqnI7OFuVA3AvEA_i_6--m2L720b7t48QUQM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP558094.RANskCjcNoqnI7OFuVA3AvEA_i_6--m2L720b7t48QUQM130_assertion
{
miriam-gene:2934
a
ncit:C16612
.
lld:C0699885
a
ncit:C7057
.
dgn-gda:DGN2e71e12034a3b7f888a4bd4ca826fa53
sio:SIO_000628
miriam-gene:2934
,
lld:C0699885
;
a
sio:SIO_001121
.
}
dgn-np:NP558094.RANskCjcNoqnI7OFuVA3AvEA_i_6--m2L720b7t48QUQM130_provenance
{
dgn-np:NP558094.RANskCjcNoqnI7OFuVA3AvEA_i_6--m2L720b7t48QUQM130_assertion
dcterms:description
"[These results suggest that nucleosome accessibility through histone deacetylation and structural changes (DMS hypersensitivity and stem loop structure) in the promoter region form the basis of the mechanism leading to the silencing of gelsolin gene in human bladder cancer.]. 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:15300799
;
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:NP558094.RANskCjcNoqnI7OFuVA3AvEA_i_6--m2L720b7t48QUQM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:36+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" .
}