@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc
> .
@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:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_head
{
this:
np:hasAssertion
dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_assertion
;
np:hasProvenance
dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_provenance
;
np:hasPublicationInfo
dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_assertion
a
np:Assertion
.
dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_provenance
a
np:Provenance
.
dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_assertion
{
miriam-gene:1869
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN096ae7f9fdc41c3485715c966e30d34a
sio:SIO_000628
miriam-gene:1869
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_provenance
{
dgn-np:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_assertion
dcterms:description
"[Possible reasons for E2F1 mediated aggressiveness are defects in cell death pathways caused by epigenetic inactivation of important tumor suppressor genes, which often occur in late stage cancer and contribute to chemoresistance.]. 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:23377972
;
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:NP389524.RACk0dUG9hOJ01Pn7pUnCD7RHX_zOyuCF10-qrkiHajTc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:52+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" .
}