@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP287281.RAtUpcCjL2zmWc8YEppu2Cx4U1L7BsfZ5fMk7NnjDar0E
> .
@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:NP287281.RAtUpcCjL2zmWc8YEppu2Cx4U1L7BsfZ5fMk7NnjDar0E130_head
{
this:
np:hasAssertion
dgn-np:NP287281.RAtUpcCjL2zmWc8YEppu2Cx4U1L7BsfZ5fMk7NnjDar0E130_assertion
;
np:hasProvenance
dgn-np:NP287281.RAtUpcCjL2zmWc8YEppu2Cx4U1L7BsfZ5fMk7NnjDar0E130_provenance
;
np:hasPublicationInfo
dgn-np:NP287281.RAtUpcCjL2zmWc8YEppu2Cx4U1L7BsfZ5fMk7NnjDar0E130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP287281.RAtUpcCjL2zmWc8YEppu2Cx4U1L7BsfZ5fMk7NnjDar0E130_assertion
a
np:Assertion
.
dgn-np:NP287281.RAtUpcCjL2zmWc8YEppu2Cx4U1L7BsfZ5fMk7NnjDar0E130_provenance
a
np:Provenance
.
dgn-np:NP287281.RAtUpcCjL2zmWc8YEppu2Cx4U1L7BsfZ5fMk7NnjDar0E130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP287281.RAtUpcCjL2zmWc8YEppu2Cx4U1L7BsfZ5fMk7NnjDar0E130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0699885
a
ncit:C7057
.
dgn-gda:DGNf36df873f9d4154cc6cc8677a37963ec
sio:SIO_000628
miriam-gene:1029
,
lld:C0699885
;
a
sio:SIO_001121
.
}
dgn-np:NP287281.RAtUpcCjL2zmWc8YEppu2Cx4U1L7BsfZ5fMk7NnjDar0E130_provenance
{
dgn-np:NP287281.RAtUpcCjL2zmWc8YEppu2Cx4U1L7BsfZ5fMk7NnjDar0E130_assertion
dcterms:description
"[These results strongly support the hypothesis that the RB nuclear overexpression recently associated with poor prognosis in bladder cancer is also associated with loss of p16 function and implies that loss of p16 function could be equally deleterious as RB loss in bladder and likely other cancers.]. 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:10022125
;
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:NP287281.RAtUpcCjL2zmWc8YEppu2Cx4U1L7BsfZ5fMk7NnjDar0E130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:43+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" .
}