@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP437289.RAZtLckMKO4Oo6E9v2Zs1HCPyJrpNFQMB8q6L38GsELgo
> .
@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:NP437289.RAZtLckMKO4Oo6E9v2Zs1HCPyJrpNFQMB8q6L38GsELgo130_head
{
this:
np:hasAssertion
dgn-np:NP437289.RAZtLckMKO4Oo6E9v2Zs1HCPyJrpNFQMB8q6L38GsELgo130_assertion
;
np:hasProvenance
dgn-np:NP437289.RAZtLckMKO4Oo6E9v2Zs1HCPyJrpNFQMB8q6L38GsELgo130_provenance
;
np:hasPublicationInfo
dgn-np:NP437289.RAZtLckMKO4Oo6E9v2Zs1HCPyJrpNFQMB8q6L38GsELgo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP437289.RAZtLckMKO4Oo6E9v2Zs1HCPyJrpNFQMB8q6L38GsELgo130_assertion
a
np:Assertion
.
dgn-np:NP437289.RAZtLckMKO4Oo6E9v2Zs1HCPyJrpNFQMB8q6L38GsELgo130_provenance
a
np:Provenance
.
dgn-np:NP437289.RAZtLckMKO4Oo6E9v2Zs1HCPyJrpNFQMB8q6L38GsELgo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP437289.RAZtLckMKO4Oo6E9v2Zs1HCPyJrpNFQMB8q6L38GsELgo130_assertion
{
miriam-gene:6422
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGN84963fd38c93b54e629c5de0f42d34d7
sio:SIO_000628
miriam-gene:6422
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP437289.RAZtLckMKO4Oo6E9v2Zs1HCPyJrpNFQMB8q6L38GsELgo130_provenance
{
dgn-np:NP437289.RAZtLckMKO4Oo6E9v2Zs1HCPyJrpNFQMB8q6L38GsELgo130_assertion
dcterms:description
"[We propose that this gene repression may be caused by gene promoter hypermethylation, as in the case of UCHL1 and SFRP1, suggesting that this epigenetic event, together with loss of specific chromosomal regions, may play an important role in meningioma progression and recurrence.]. 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:22964784
;
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:NP437289.RAZtLckMKO4Oo6E9v2Zs1HCPyJrpNFQMB8q6L38GsELgo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:19+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" .
}