@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP759872.RAkt0aTQnz3ezZ2pBDBh_wFib08dmKgH_2Zco921o_LRs
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP759872.RAkt0aTQnz3ezZ2pBDBh_wFib08dmKgH_2Zco921o_LRs130_assertion
;
np:hasProvenance
dgn-np:NP759872.RAkt0aTQnz3ezZ2pBDBh_wFib08dmKgH_2Zco921o_LRs130_provenance
;
np:hasPublicationInfo
dgn-np:NP759872.RAkt0aTQnz3ezZ2pBDBh_wFib08dmKgH_2Zco921o_LRs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP759872.RAkt0aTQnz3ezZ2pBDBh_wFib08dmKgH_2Zco921o_LRs130_assertion
a
np:Assertion
.
dgn-np:NP759872.RAkt0aTQnz3ezZ2pBDBh_wFib08dmKgH_2Zco921o_LRs130_provenance
a
np:Provenance
.
dgn-np:NP759872.RAkt0aTQnz3ezZ2pBDBh_wFib08dmKgH_2Zco921o_LRs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP759872.RAkt0aTQnz3ezZ2pBDBh_wFib08dmKgH_2Zco921o_LRs130_assertion
{
miriam-gene:6422
a
ncit:C16612
.
lld:C1762616
a
ncit:C7057
.
dgn-gda:DGN6f24f92f58c33df4cc4087e2e6e63fec
sio:SIO_000628
miriam-gene:6422
,
lld:C1762616
;
a
sio:SIO_001121
.
}
dgn-np:NP759872.RAkt0aTQnz3ezZ2pBDBh_wFib08dmKgH_2Zco921o_LRs130_provenance
{
dgn-np:NP759872.RAkt0aTQnz3ezZ2pBDBh_wFib08dmKgH_2Zco921o_LRs130_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:NP759872.RAkt0aTQnz3ezZ2pBDBh_wFib08dmKgH_2Zco921o_LRs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}