@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP191787.RAyCtPDIKw8hcXG8aRGcdwMnx1zAjwWP6qMSI93O3N3Zk
> .
@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:NP191787.RAyCtPDIKw8hcXG8aRGcdwMnx1zAjwWP6qMSI93O3N3Zk130_head
{
this:
np:hasAssertion
dgn-np:NP191787.RAyCtPDIKw8hcXG8aRGcdwMnx1zAjwWP6qMSI93O3N3Zk130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP191787.RAyCtPDIKw8hcXG8aRGcdwMnx1zAjwWP6qMSI93O3N3Zk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP191787.RAyCtPDIKw8hcXG8aRGcdwMnx1zAjwWP6qMSI93O3N3Zk130_assertion
a
np:Assertion
.
dgn-np:NP191787.RAyCtPDIKw8hcXG8aRGcdwMnx1zAjwWP6qMSI93O3N3Zk130_provenance
a
np:Provenance
.
dgn-np:NP191787.RAyCtPDIKw8hcXG8aRGcdwMnx1zAjwWP6qMSI93O3N3Zk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP191787.RAyCtPDIKw8hcXG8aRGcdwMnx1zAjwWP6qMSI93O3N3Zk130_assertion
{
miriam-gene:7813
a
ncit:C16612
.
lld:C0700095
a
ncit:C7057
.
dgn-gda:DGN20528272d02ba16270495ff443f3673a
sio:SIO_000628
miriam-gene:7813
,
lld:C0700095
;
a
sio:SIO_001121
.
}
dgn-np:NP191787.RAyCtPDIKw8hcXG8aRGcdwMnx1zAjwWP6qMSI93O3N3Zk130_provenance
{
dgn-np:NP191787.RAyCtPDIKw8hcXG8aRGcdwMnx1zAjwWP6qMSI93O3N3Zk130_assertion
dcterms:description
"[Here, we describe the recent acquisition of the NBPF1 promoter from an unrelated gene, and remarkably, both the donor (EVI5) and acceptor (NBPF1) genes are disrupted by constitutional translocations in patients with neuroblastoma, suggesting a functional link between these genes and the disease.]. 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:19282512
;
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:NP191787.RAyCtPDIKw8hcXG8aRGcdwMnx1zAjwWP6qMSI93O3N3Zk130_publicationInfo
{
this:
dcterms:created
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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
<
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> , <
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> , <
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
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"v2.1.0" .
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