@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP80929.RAR60pCPDe5CzCerK2GyLSkhjGDD1pRtHFF1DgYjWP_D8
> .
@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 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:NP80929.RAR60pCPDe5CzCerK2GyLSkhjGDD1pRtHFF1DgYjWP_D8130_head
{
this:
np:hasAssertion
dgn-np:NP80929.RAR60pCPDe5CzCerK2GyLSkhjGDD1pRtHFF1DgYjWP_D8130_assertion
;
np:hasProvenance
dgn-np:NP80929.RAR60pCPDe5CzCerK2GyLSkhjGDD1pRtHFF1DgYjWP_D8130_provenance
;
np:hasPublicationInfo
dgn-np:NP80929.RAR60pCPDe5CzCerK2GyLSkhjGDD1pRtHFF1DgYjWP_D8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP80929.RAR60pCPDe5CzCerK2GyLSkhjGDD1pRtHFF1DgYjWP_D8130_assertion
a
np:Assertion
.
dgn-np:NP80929.RAR60pCPDe5CzCerK2GyLSkhjGDD1pRtHFF1DgYjWP_D8130_provenance
a
np:Provenance
.
dgn-np:NP80929.RAR60pCPDe5CzCerK2GyLSkhjGDD1pRtHFF1DgYjWP_D8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP80929.RAR60pCPDe5CzCerK2GyLSkhjGDD1pRtHFF1DgYjWP_D8130_assertion
{
miriam-gene:7015
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGNf320e09ac3e1f66038da71a475835413
sio:SIO_000628
miriam-gene:7015
,
lld:C0242379
;
a
sio:SIO_001122
.
}
dgn-np:NP80929.RAR60pCPDe5CzCerK2GyLSkhjGDD1pRtHFF1DgYjWP_D8130_provenance
{
dgn-np:NP80929.RAR60pCPDe5CzCerK2GyLSkhjGDD1pRtHFF1DgYjWP_D8130_assertion
dc:description
"[Telomerase functional polymorphism in the hTERT gene may contribute as a prognostic factor in NSCLC patients. Our findings indicate that hTERT genetic variants, by modulating telomere length, may confer an advantage in chemotherapy response. The assessment of telomerase genetic variants could supplement prognosis of survival in the course of NSCLC and may be a promising molecular marker of treatment response in these patients.]. 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:20606038
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP80929.RAR60pCPDe5CzCerK2GyLSkhjGDD1pRtHFF1DgYjWP_D8130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:40+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}