@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP587229.RAr4CUS-5J9rMPZRWEFtv5QDERERsl29jZbvDjy2QU-7Y
> .
@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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP587229.RAr4CUS-5J9rMPZRWEFtv5QDERERsl29jZbvDjy2QU-7Y130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP587229.RAr4CUS-5J9rMPZRWEFtv5QDERERsl29jZbvDjy2QU-7Y130_assertion
a
np:Assertion
.
dgn-np:NP587229.RAr4CUS-5J9rMPZRWEFtv5QDERERsl29jZbvDjy2QU-7Y130_provenance
a
np:Provenance
.
dgn-np:NP587229.RAr4CUS-5J9rMPZRWEFtv5QDERERsl29jZbvDjy2QU-7Y130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:4169
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN5cd3aedb3a684d1043a844a14873822f
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miriam-gene:4169
,
lld:C0006826
;
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.
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dgn-np:NP587229.RAr4CUS-5J9rMPZRWEFtv5QDERERsl29jZbvDjy2QU-7Y130_provenance
{
dgn-np:NP587229.RAr4CUS-5J9rMPZRWEFtv5QDERERsl29jZbvDjy2QU-7Y130_assertion
dcterms:description
"[Since not all gene expression changes observed in a tumor are causal to cancer development, we demonstrate an approach based on multiple concerted disruption (MCD) analysis of genes that facilitates the rational deduction of aberrant genes and pathways, which otherwise would be overlooked in single genomic dimension investigations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
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sio:SIO_000772
miriam-pubmed:20478067
;
prov:wasDerivedFrom
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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 .
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dgn-np:NP587229.RAr4CUS-5J9rMPZRWEFtv5QDERERsl29jZbvDjy2QU-7Y130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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> , <
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> , <
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pav:createdBy
<
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