@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP390807.RAD2ae9OXwPGU9hcPzaUL5KGXLKeBOuf_PkJ1tLCZWLUY
> .
@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:NP390807.RAD2ae9OXwPGU9hcPzaUL5KGXLKeBOuf_PkJ1tLCZWLUY130_head
{
this:
np:hasAssertion
dgn-np:NP390807.RAD2ae9OXwPGU9hcPzaUL5KGXLKeBOuf_PkJ1tLCZWLUY130_assertion
;
np:hasProvenance
dgn-np:NP390807.RAD2ae9OXwPGU9hcPzaUL5KGXLKeBOuf_PkJ1tLCZWLUY130_provenance
;
np:hasPublicationInfo
dgn-np:NP390807.RAD2ae9OXwPGU9hcPzaUL5KGXLKeBOuf_PkJ1tLCZWLUY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP390807.RAD2ae9OXwPGU9hcPzaUL5KGXLKeBOuf_PkJ1tLCZWLUY130_assertion
a
np:Assertion
.
dgn-np:NP390807.RAD2ae9OXwPGU9hcPzaUL5KGXLKeBOuf_PkJ1tLCZWLUY130_provenance
a
np:Provenance
.
dgn-np:NP390807.RAD2ae9OXwPGU9hcPzaUL5KGXLKeBOuf_PkJ1tLCZWLUY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP390807.RAD2ae9OXwPGU9hcPzaUL5KGXLKeBOuf_PkJ1tLCZWLUY130_assertion
{
miriam-gene:1030
a
ncit:C16612
.
lld:C0017636
a
ncit:C7057
.
dgn-gda:DGN0b30d5598fde247f5cc9800c843c13a1
sio:SIO_000628
miriam-gene:1030
,
lld:C0017636
;
a
sio:SIO_001121
.
}
dgn-np:NP390807.RAD2ae9OXwPGU9hcPzaUL5KGXLKeBOuf_PkJ1tLCZWLUY130_provenance
{
dgn-np:NP390807.RAD2ae9OXwPGU9hcPzaUL5KGXLKeBOuf_PkJ1tLCZWLUY130_assertion
dcterms:description
"[Our results indicate that loss of the p16 and p15 genes may be involved in tumor progression in human gliomas, especially in the development of glioblastoma, that this loss may give growth advantage to the cells in culture, and that it is not the result of culture artifacts.]. 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:7497469
;
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:NP390807.RAD2ae9OXwPGU9hcPzaUL5KGXLKeBOuf_PkJ1tLCZWLUY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:53+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" .
}