@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP483512.RA1iJAwtQtaHF8i5NZxAkrn8GD92E6uF6pV2CRLVtf_nM
> .
@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:NP483512.RA1iJAwtQtaHF8i5NZxAkrn8GD92E6uF6pV2CRLVtf_nM130_head
{
this:
np:hasAssertion
dgn-np:NP483512.RA1iJAwtQtaHF8i5NZxAkrn8GD92E6uF6pV2CRLVtf_nM130_assertion
;
np:hasProvenance
dgn-np:NP483512.RA1iJAwtQtaHF8i5NZxAkrn8GD92E6uF6pV2CRLVtf_nM130_provenance
;
np:hasPublicationInfo
dgn-np:NP483512.RA1iJAwtQtaHF8i5NZxAkrn8GD92E6uF6pV2CRLVtf_nM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP483512.RA1iJAwtQtaHF8i5NZxAkrn8GD92E6uF6pV2CRLVtf_nM130_assertion
a
np:Assertion
.
dgn-np:NP483512.RA1iJAwtQtaHF8i5NZxAkrn8GD92E6uF6pV2CRLVtf_nM130_provenance
a
np:Provenance
.
dgn-np:NP483512.RA1iJAwtQtaHF8i5NZxAkrn8GD92E6uF6pV2CRLVtf_nM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP483512.RA1iJAwtQtaHF8i5NZxAkrn8GD92E6uF6pV2CRLVtf_nM130_assertion
{
miriam-gene:1869
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN2f372207a3d94207cca11327b4d85d3c
sio:SIO_000628
miriam-gene:1869
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP483512.RA1iJAwtQtaHF8i5NZxAkrn8GD92E6uF6pV2CRLVtf_nM130_provenance
{
dgn-np:NP483512.RA1iJAwtQtaHF8i5NZxAkrn8GD92E6uF6pV2CRLVtf_nM130_assertion
dcterms:description
"[These data demonstrate that the Rb/E2F1 axis exerts essential functions not only in maintaining epidermal homoeostasis, but also in suppressing tumour development in epidermis, and that the disruption of this pathway may induce tumour progression through specific alteration of developmental programs.]. 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:22890321
;
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:NP483512.RA1iJAwtQtaHF8i5NZxAkrn8GD92E6uF6pV2CRLVtf_nM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:49+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" .
}