@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY
> .
@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:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_head
{
this:
np:hasAssertion
dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_assertion
;
np:hasProvenance
dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_provenance
;
np:hasPublicationInfo
dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_assertion
a
np:Assertion
.
dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_provenance
a
np:Provenance
.
dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_assertion
{
miriam-gene:2475
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN3c0e3e39099a17d2ac5a634f979bb7af
sio:SIO_000628
miriam-gene:2475
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_provenance
{
dgn-np:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_assertion
dcterms:description
"[Most notably, the severe chromosomal abnormality did not cause cell death owing to the activation of AKT pathway, including elevated levels of phosphorylated AKT and mammalian target of rapamycin, and nuclear accumulation of cyclin D1, which enabled continuous proliferation of the tetraploid 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:16715125
;
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:NP518286.RAtbPFyEIHLVcUbIiM7AgrCPNyTwY0kPL_NwdiXA3m2kY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:08+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" .
}