@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP304684.RAuUoaCwqZuZRairPr2upwG_FeB1s6-X1VPp7kZBF94rU
> .
@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:NP304684.RAuUoaCwqZuZRairPr2upwG_FeB1s6-X1VPp7kZBF94rU130_head
{
this:
np:hasAssertion
dgn-np:NP304684.RAuUoaCwqZuZRairPr2upwG_FeB1s6-X1VPp7kZBF94rU130_assertion
;
np:hasProvenance
dgn-np:NP304684.RAuUoaCwqZuZRairPr2upwG_FeB1s6-X1VPp7kZBF94rU130_provenance
;
np:hasPublicationInfo
dgn-np:NP304684.RAuUoaCwqZuZRairPr2upwG_FeB1s6-X1VPp7kZBF94rU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP304684.RAuUoaCwqZuZRairPr2upwG_FeB1s6-X1VPp7kZBF94rU130_assertion
a
np:Assertion
.
dgn-np:NP304684.RAuUoaCwqZuZRairPr2upwG_FeB1s6-X1VPp7kZBF94rU130_provenance
a
np:Provenance
.
dgn-np:NP304684.RAuUoaCwqZuZRairPr2upwG_FeB1s6-X1VPp7kZBF94rU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP304684.RAuUoaCwqZuZRairPr2upwG_FeB1s6-X1VPp7kZBF94rU130_assertion
{
miriam-gene:84260
a
ncit:C16612
.
lld:C0035335
a
ncit:C7057
.
dgn-gda:DGNd79de37721f459c82bd91fa2cd8245f4
sio:SIO_000628
miriam-gene:84260
,
lld:C0035335
;
a
sio:SIO_001121
.
}
dgn-np:NP304684.RAuUoaCwqZuZRairPr2upwG_FeB1s6-X1VPp7kZBF94rU130_provenance
{
dgn-np:NP304684.RAuUoaCwqZuZRairPr2upwG_FeB1s6-X1VPp7kZBF94rU130_assertion
dcterms:description
"[It is becoming clear that a common feature of cancer cells is the abrogation of cell cycle checkpoints, either by aberrant expression of positive regulators (for example, cyclins and CDKs) or the loss of negative regulators, including p21Cip1 through loss of function of its transcriptional activator p53, or deletion or mutation of p16ink4A (multiple tumor suppressor 1/CDKN2) and the retinoblastoma tumor suppressor protein.]. 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:9149259
;
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:NP304684.RAuUoaCwqZuZRairPr2upwG_FeB1s6-X1VPp7kZBF94rU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:55+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" .
}