@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM
> .
@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:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_head
{
this:
np:hasAssertion
dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_assertion
;
np:hasProvenance
dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_provenance
;
np:hasPublicationInfo
dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_assertion
a
np:Assertion
.
dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_provenance
a
np:Provenance
.
dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_assertion
{
miriam-gene:4771
a
ncit:C16612
.
lld:C0027859
a
ncit:C7057
.
dgn-gda:DGNbc644034a7b57fa4103f1c756c2257d5
sio:SIO_000628
miriam-gene:4771
,
lld:C0027859
;
a
sio:SIO_001121
.
}
dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_provenance
{
dgn-np:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_assertion
dcterms:description
"[Importantly, high level amplifications have been observed on 16p and 16q as well as on 9q, suggesting the possible involvement of several oncogenes in the tumorigenesis of VS. Our data suggest the involvement of various oncogenes and tumor suppressor genes might play a role in the genesis of the vestibular schwannomas apart from the inactivation of the NF2 gene.]. 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:20872275
;
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:NP189865.RAW7mIEImkYm55AubdYCqUAvx67516V-ih_OxkiFgtsgM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}