@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP851666.RAnsvV73FO0HTk5Y8FYQgkovzT-AfLbGF5m5CeLV-tTh8
> .
@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:NP851666.RAnsvV73FO0HTk5Y8FYQgkovzT-AfLbGF5m5CeLV-tTh8130_head
{
this:
np:hasAssertion
dgn-np:NP851666.RAnsvV73FO0HTk5Y8FYQgkovzT-AfLbGF5m5CeLV-tTh8130_assertion
;
np:hasProvenance
dgn-np:NP851666.RAnsvV73FO0HTk5Y8FYQgkovzT-AfLbGF5m5CeLV-tTh8130_provenance
;
np:hasPublicationInfo
dgn-np:NP851666.RAnsvV73FO0HTk5Y8FYQgkovzT-AfLbGF5m5CeLV-tTh8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP851666.RAnsvV73FO0HTk5Y8FYQgkovzT-AfLbGF5m5CeLV-tTh8130_assertion
a
np:Assertion
.
dgn-np:NP851666.RAnsvV73FO0HTk5Y8FYQgkovzT-AfLbGF5m5CeLV-tTh8130_provenance
a
np:Provenance
.
dgn-np:NP851666.RAnsvV73FO0HTk5Y8FYQgkovzT-AfLbGF5m5CeLV-tTh8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP851666.RAnsvV73FO0HTk5Y8FYQgkovzT-AfLbGF5m5CeLV-tTh8130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C1519214
a
ncit:C7057
.
dgn-gda:DGNec968d01ed556a946d84599493ad7fcf
sio:SIO_000628
miriam-gene:1029
,
lld:C1519214
;
a
sio:SIO_001121
.
}
dgn-np:NP851666.RAnsvV73FO0HTk5Y8FYQgkovzT-AfLbGF5m5CeLV-tTh8130_provenance
{
dgn-np:NP851666.RAnsvV73FO0HTk5Y8FYQgkovzT-AfLbGF5m5CeLV-tTh8130_assertion
dcterms:description
"[These results suggest that aberrant p14ARF expression due to homozygous deletion or promoter hypermethylation is associated with the evolution of both primary and secondary glioblastomas, and that p14ARF promoter methylation is an early event in subset of astrocytomas that undergo malignant progression to secondary glioblastoma.]. 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:11303791
;
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:NP851666.RAnsvV73FO0HTk5Y8FYQgkovzT-AfLbGF5m5CeLV-tTh8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:40+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" .
}