@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP389619.RAL8tcZoxwlyAv7csGO5fEoMP7U-ws0lxe8FiuZe7CyZg
> .
@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:NP389619.RAL8tcZoxwlyAv7csGO5fEoMP7U-ws0lxe8FiuZe7CyZg130_head
{
this:
np:hasAssertion
dgn-np:NP389619.RAL8tcZoxwlyAv7csGO5fEoMP7U-ws0lxe8FiuZe7CyZg130_assertion
;
np:hasProvenance
dgn-np:NP389619.RAL8tcZoxwlyAv7csGO5fEoMP7U-ws0lxe8FiuZe7CyZg130_provenance
;
np:hasPublicationInfo
dgn-np:NP389619.RAL8tcZoxwlyAv7csGO5fEoMP7U-ws0lxe8FiuZe7CyZg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP389619.RAL8tcZoxwlyAv7csGO5fEoMP7U-ws0lxe8FiuZe7CyZg130_assertion
a
np:Assertion
.
dgn-np:NP389619.RAL8tcZoxwlyAv7csGO5fEoMP7U-ws0lxe8FiuZe7CyZg130_provenance
a
np:Provenance
.
dgn-np:NP389619.RAL8tcZoxwlyAv7csGO5fEoMP7U-ws0lxe8FiuZe7CyZg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP389619.RAL8tcZoxwlyAv7csGO5fEoMP7U-ws0lxe8FiuZe7CyZg130_assertion
{
miriam-gene:3621
a
ncit:C16612
.
lld:C0006118
a
ncit:C7057
.
dgn-gda:DGN4323043f56cd6c63503b72ec56feb49a
sio:SIO_000628
miriam-gene:3621
,
lld:C0006118
;
a
sio:SIO_001121
.
}
dgn-np:NP389619.RAL8tcZoxwlyAv7csGO5fEoMP7U-ws0lxe8FiuZe7CyZg130_provenance
{
dgn-np:NP389619.RAL8tcZoxwlyAv7csGO5fEoMP7U-ws0lxe8FiuZe7CyZg130_assertion
dcterms:description
"[Our data indicate that although mutations of ING1 seem to be infrequent in human brain tumors, deregulated expression and mislocalization of ING1 proteins, particularly the p33ING1b isoform, are common events in gliomas and glioblastomas.]. 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:14676120
;
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:NP389619.RAL8tcZoxwlyAv7csGO5fEoMP7U-ws0lxe8FiuZe7CyZg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:52+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" .
}