@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP163014.RAiHnG_ZdhYhANcUU2K6cB_FsS8kjAROFbwPXujsixa8A
> .
@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:NP163014.RAiHnG_ZdhYhANcUU2K6cB_FsS8kjAROFbwPXujsixa8A130_head
{
this:
np:hasAssertion
dgn-np:NP163014.RAiHnG_ZdhYhANcUU2K6cB_FsS8kjAROFbwPXujsixa8A130_assertion
;
np:hasProvenance
dgn-np:NP163014.RAiHnG_ZdhYhANcUU2K6cB_FsS8kjAROFbwPXujsixa8A130_provenance
;
np:hasPublicationInfo
dgn-np:NP163014.RAiHnG_ZdhYhANcUU2K6cB_FsS8kjAROFbwPXujsixa8A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP163014.RAiHnG_ZdhYhANcUU2K6cB_FsS8kjAROFbwPXujsixa8A130_assertion
a
np:Assertion
.
dgn-np:NP163014.RAiHnG_ZdhYhANcUU2K6cB_FsS8kjAROFbwPXujsixa8A130_provenance
a
np:Provenance
.
dgn-np:NP163014.RAiHnG_ZdhYhANcUU2K6cB_FsS8kjAROFbwPXujsixa8A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP163014.RAiHnG_ZdhYhANcUU2K6cB_FsS8kjAROFbwPXujsixa8A130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGN502e9a304e79a45c4d97b3233f900ac5
sio:SIO_000628
miriam-gene:1029
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP163014.RAiHnG_ZdhYhANcUU2K6cB_FsS8kjAROFbwPXujsixa8A130_provenance
{
dgn-np:NP163014.RAiHnG_ZdhYhANcUU2K6cB_FsS8kjAROFbwPXujsixa8A130_assertion
dcterms:description
"[Alternatively, since the p16, retinoblastoma (RB), and CDK4 genes have been implicated in malignant progression, detection of losses or amplifications of these genes in gliomas could be diagnostically, prognostically, and therapeutically important.]. 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:10587703
;
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:NP163014.RAiHnG_ZdhYhANcUU2K6cB_FsS8kjAROFbwPXujsixa8A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:28+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" .
}