@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP348329.RAwi2agzWvsBRzswqdDItJyMaexoaVctWbH8pCFm8Okew
> .
@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:NP348329.RAwi2agzWvsBRzswqdDItJyMaexoaVctWbH8pCFm8Okew130_head
{
this:
np:hasAssertion
dgn-np:NP348329.RAwi2agzWvsBRzswqdDItJyMaexoaVctWbH8pCFm8Okew130_assertion
;
np:hasProvenance
dgn-np:NP348329.RAwi2agzWvsBRzswqdDItJyMaexoaVctWbH8pCFm8Okew130_provenance
;
np:hasPublicationInfo
dgn-np:NP348329.RAwi2agzWvsBRzswqdDItJyMaexoaVctWbH8pCFm8Okew130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP348329.RAwi2agzWvsBRzswqdDItJyMaexoaVctWbH8pCFm8Okew130_assertion
a
np:Assertion
.
dgn-np:NP348329.RAwi2agzWvsBRzswqdDItJyMaexoaVctWbH8pCFm8Okew130_provenance
a
np:Provenance
.
dgn-np:NP348329.RAwi2agzWvsBRzswqdDItJyMaexoaVctWbH8pCFm8Okew130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP348329.RAwi2agzWvsBRzswqdDItJyMaexoaVctWbH8pCFm8Okew130_assertion
{
miriam-gene:4613
a
ncit:C16612
.
lld:C0085281
a
ncit:C7057
.
dgn-gda:DGNab53bdf51ae688b3e5fc88cb76ae53b6
sio:SIO_000628
miriam-gene:4613
,
lld:C0085281
;
a
sio:SIO_001121
.
}
dgn-np:NP348329.RAwi2agzWvsBRzswqdDItJyMaexoaVctWbH8pCFm8Okew130_provenance
{
dgn-np:NP348329.RAwi2agzWvsBRzswqdDItJyMaexoaVctWbH8pCFm8Okew130_assertion
dcterms:description
"[Taken together, our data indicate that focal DNA copy number imbalances in neuroblastoma (1) target genes that are implicated in MYCN signaling, possibly selected to reinforce MYCN oncogene addiction and (2) serve as a resource for identifying new molecular targets for treatment.]. 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:23308108
;
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:NP348329.RAwi2agzWvsBRzswqdDItJyMaexoaVctWbH8pCFm8Okew130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:24+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" .
}