@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_assertion
a
np:Assertion
.
dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_provenance
a
np:Provenance
.
dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:1663
a
ncit:C16612
.
lld:C0278883
a
ncit:C7057
.
dgn-gda:DGNd7b906df182c48263779d9f88f1ecc4d
sio:SIO_000628
miriam-gene:1663
,
lld:C0278883
;
a
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.
}
dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_provenance
{
dgn-np:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_assertion
dcterms:description
"[In this report, we show that the helicase DDX11 is expressed at high levels in primary and metastatic melanoma, and that interfering with its expression leads to severe chromosome segregation defects, telomere shortening, and massive melanoma cell apoptosis.]. 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:23116066
;
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:NP881998.RAXq3V-dzKjLXmQA3XX1TNw2BzDA4um4rhyZLhyBewz-o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:59+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
<
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> , <
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" .
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pav:version
"v2.1.0" .
}