@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP637370.RAv5tUnM-49Q8cQh50Z9t3l9Iz-LtnKVIQvWgIZ4gjw1s
> .
@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:NP637370.RAv5tUnM-49Q8cQh50Z9t3l9Iz-LtnKVIQvWgIZ4gjw1s130_head
{
this:
np:hasAssertion
dgn-np:NP637370.RAv5tUnM-49Q8cQh50Z9t3l9Iz-LtnKVIQvWgIZ4gjw1s130_assertion
;
np:hasProvenance
dgn-np:NP637370.RAv5tUnM-49Q8cQh50Z9t3l9Iz-LtnKVIQvWgIZ4gjw1s130_provenance
;
np:hasPublicationInfo
dgn-np:NP637370.RAv5tUnM-49Q8cQh50Z9t3l9Iz-LtnKVIQvWgIZ4gjw1s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP637370.RAv5tUnM-49Q8cQh50Z9t3l9Iz-LtnKVIQvWgIZ4gjw1s130_assertion
a
np:Assertion
.
dgn-np:NP637370.RAv5tUnM-49Q8cQh50Z9t3l9Iz-LtnKVIQvWgIZ4gjw1s130_provenance
a
np:Provenance
.
dgn-np:NP637370.RAv5tUnM-49Q8cQh50Z9t3l9Iz-LtnKVIQvWgIZ4gjw1s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP637370.RAv5tUnM-49Q8cQh50Z9t3l9Iz-LtnKVIQvWgIZ4gjw1s130_assertion
{
miriam-gene:8771
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN21990df26139e526f81dbe5cdfd78ad1
sio:SIO_000628
miriam-gene:8771
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP637370.RAv5tUnM-49Q8cQh50Z9t3l9Iz-LtnKVIQvWgIZ4gjw1s130_provenance
{
dgn-np:NP637370.RAv5tUnM-49Q8cQh50Z9t3l9Iz-LtnKVIQvWgIZ4gjw1s130_assertion
dcterms:description
"[Amplification of HCK, TNFRSF6B and DIDO1 genes included in retained regions associated with loss of tumour suppressor genes in deleted regions could explain cell tumour progression and possibly the less favourable prognosis of ider(20q) compared with del(20q).]. 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:19036015
;
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:NP637370.RAv5tUnM-49Q8cQh50Z9t3l9Iz-LtnKVIQvWgIZ4gjw1s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:24+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" .
}