@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw
> .
@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:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_head
{
this:
np:hasAssertion
dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_assertion
;
np:hasProvenance
dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_provenance
;
np:hasPublicationInfo
dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_assertion
a
np:Assertion
.
dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_provenance
a
np:Provenance
.
dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_assertion
{
miriam-gene:5925
a
ncit:C16612
.
lld:C0001418
a
ncit:C7057
.
dgn-gda:DGNfdb1bb51cc28c9f1a2ee793589c9c447
sio:SIO_000628
miriam-gene:5925
,
lld:C0001418
;
a
sio:SIO_001121
.
}
dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_provenance
{
dgn-np:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_assertion
dcterms:description
"[We found that half (7 of 14) of lung adenocarcinomas with high telomerase activity showed neither TP53 nor RB1 deletion, while all squamous cell carcinomas and SCLCs with high telomerase activity showed loss of heterozygosity of at least one, if not both, of these suppressor oncogenes, indicating that these genetic aberrations are not required in activation of telomerase in a unique subset of adenocarcinoma.]. 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:17487398
;
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:NP771465.RAmHqgMLJJNa6JeW5BOSsiTyL6-Wt19rj-FLWY5F99tRw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:46+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" .
}