@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP178816.RANOM7m69xxReRyZeks0_ewBCCUKn_PLrC9Dyas7SItAA
> .
@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#
> .
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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:
np:hasAssertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP178816.RANOM7m69xxReRyZeks0_ewBCCUKn_PLrC9Dyas7SItAA130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP178816.RANOM7m69xxReRyZeks0_ewBCCUKn_PLrC9Dyas7SItAA130_assertion
a
np:Assertion
.
dgn-np:NP178816.RANOM7m69xxReRyZeks0_ewBCCUKn_PLrC9Dyas7SItAA130_provenance
a
np:Provenance
.
dgn-np:NP178816.RANOM7m69xxReRyZeks0_ewBCCUKn_PLrC9Dyas7SItAA130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:4360
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNf246aa916f373764bac5f0684cd9ac05
sio:SIO_000628
miriam-gene:4360
,
lld:C0027651
;
a
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.
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dgn-np:NP178816.RANOM7m69xxReRyZeks0_ewBCCUKn_PLrC9Dyas7SItAA130_provenance
{
dgn-np:NP178816.RANOM7m69xxReRyZeks0_ewBCCUKn_PLrC9Dyas7SItAA130_assertion
dcterms:description
"[Our findings suggest that in a rare subset of patients, inactivation of the genes of the MMR pathway is likely an important step in the molecular pathogenesis of DLBCL and does not involve the same molecular mechanisms as other common neoplasms with MMR deficiency.]. 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:23066952
;
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 .
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dgn-np:NP178816.RANOM7m69xxReRyZeks0_ewBCCUKn_PLrC9Dyas7SItAA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:37+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
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pav:authoredBy
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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