@prefix semsc: <
http://semanticscience.org/resource/
> .
@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@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 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:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_head
{
this:
np:hasAssertion
dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_assertion
;
np:hasProvenance
dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_provenance
;
np:hasPublicationInfo
dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_assertion
a
np:Assertion
.
dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_provenance
a
np:Provenance
.
dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_assertion
{
miriam-gene:23417
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN2f7f8ddde37e25f2d81445389d2eb839
semsc:SIO_000628
miriam-gene:23417
,
lld:C0006826
;
a
semsc:SIO_001121
.
}
dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_provenance
{
dgn-np:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_assertion
dct: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
dgn-void:source_evidence_literature
;
semsc:SIO_000772
miriam-pubmed:20478067
;
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:NP205729.RAAkzVcYt64TCCOZhg09S6i9I4QwDhQs8lE6rdz-8nFs4130_publicationInfo
{
this:
dct:created
"2014-10-02T12:33:53+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
semsc:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}