@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216681.RAZemM4xXrM0UA_LxYKhF1qVWdjPsDVd87XxAQp3Lw4sM
> .
@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:NP216681.RAZemM4xXrM0UA_LxYKhF1qVWdjPsDVd87XxAQp3Lw4sM130_head
{
this:
np:hasAssertion
dgn-np:NP216681.RAZemM4xXrM0UA_LxYKhF1qVWdjPsDVd87XxAQp3Lw4sM130_assertion
;
np:hasProvenance
dgn-np:NP216681.RAZemM4xXrM0UA_LxYKhF1qVWdjPsDVd87XxAQp3Lw4sM130_provenance
;
np:hasPublicationInfo
dgn-np:NP216681.RAZemM4xXrM0UA_LxYKhF1qVWdjPsDVd87XxAQp3Lw4sM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216681.RAZemM4xXrM0UA_LxYKhF1qVWdjPsDVd87XxAQp3Lw4sM130_assertion
a
np:Assertion
.
dgn-np:NP216681.RAZemM4xXrM0UA_LxYKhF1qVWdjPsDVd87XxAQp3Lw4sM130_provenance
a
np:Provenance
.
dgn-np:NP216681.RAZemM4xXrM0UA_LxYKhF1qVWdjPsDVd87XxAQp3Lw4sM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216681.RAZemM4xXrM0UA_LxYKhF1qVWdjPsDVd87XxAQp3Lw4sM130_assertion
{
miriam-gene:7015
a
ncit:C16612
.
lld:C0023473
a
ncit:C7057
.
dgn-gda:DGN1f48d111523cb4c41654f174c013d513
sio:SIO_000628
miriam-gene:7015
,
lld:C0023473
;
a
sio:SIO_001121
.
}
dgn-np:NP216681.RAZemM4xXrM0UA_LxYKhF1qVWdjPsDVd87XxAQp3Lw4sM130_provenance
{
dgn-np:NP216681.RAZemM4xXrM0UA_LxYKhF1qVWdjPsDVd87XxAQp3Lw4sM130_assertion
dcterms:description
"[Keeping in view the fact that a single acquired genetic abnormality `Bcr-Abl chimeric gene` accompanied by elevated telomerase activity has been widely recognized to be responsible for the leukemic myelopoiesis observed in chronic myeloid leukemia (CML), the present study was addressed to understand as to how selective and specific knock-down of human telomerase reverse transcriptase (hTERT) gene within mononuclear cells derived from untreated CML subjects could influence the apoptotic, genotypic (such as Bcr-Abl; C-myc; Bcl-2; IL-6; GMCSF; IL-3; and acetylated H(3) and H(4)), and phenotypic (such as CD34 and CD89) characteristics of these cells.]. 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:18409031
;
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:NP216681.RAZemM4xXrM0UA_LxYKhF1qVWdjPsDVd87XxAQp3Lw4sM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}