@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP696857.RAt21r0vNjDANopTblwkp2tR78pxYt3rx-iKRQF8mGDf0
> .
@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:NP696857.RAt21r0vNjDANopTblwkp2tR78pxYt3rx-iKRQF8mGDf0130_head
{
this:
np:hasAssertion
dgn-np:NP696857.RAt21r0vNjDANopTblwkp2tR78pxYt3rx-iKRQF8mGDf0130_assertion
;
np:hasProvenance
dgn-np:NP696857.RAt21r0vNjDANopTblwkp2tR78pxYt3rx-iKRQF8mGDf0130_provenance
;
np:hasPublicationInfo
dgn-np:NP696857.RAt21r0vNjDANopTblwkp2tR78pxYt3rx-iKRQF8mGDf0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP696857.RAt21r0vNjDANopTblwkp2tR78pxYt3rx-iKRQF8mGDf0130_assertion
a
np:Assertion
.
dgn-np:NP696857.RAt21r0vNjDANopTblwkp2tR78pxYt3rx-iKRQF8mGDf0130_provenance
a
np:Provenance
.
dgn-np:NP696857.RAt21r0vNjDANopTblwkp2tR78pxYt3rx-iKRQF8mGDf0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP696857.RAt21r0vNjDANopTblwkp2tR78pxYt3rx-iKRQF8mGDf0130_assertion
{
miriam-gene:161291
a
ncit:C16612
.
lld:C0025286
a
ncit:C7057
.
dgn-gda:DGN44b44516c5e0793ba1e22a6207fcb572
sio:SIO_000628
miriam-gene:161291
,
lld:C0025286
;
a
sio:SIO_001121
.
}
dgn-np:NP696857.RAt21r0vNjDANopTblwkp2tR78pxYt3rx-iKRQF8mGDf0130_provenance
{
dgn-np:NP696857.RAt21r0vNjDANopTblwkp2tR78pxYt3rx-iKRQF8mGDf0130_assertion
dcterms:description
"[The signature was composed of genes involved in the cell cycle (TMEM30B, CKS2, and UCHL1) and other pathways previously described as being altered in meningiomas, that is, WNT (SFRP1 and SFRP4) and transforming growth factor-β pathways (LTBP2 and LMO4).]. 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:NP696857.RAt21r0vNjDANopTblwkp2tR78pxYt3rx-iKRQF8mGDf0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:04+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" .
}