@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP482206.RAFVEsnX12H6jLY7I9UkFgoksDBBwsBJ6RhQLsZOQMY9Q
> .
@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:NP482206.RAFVEsnX12H6jLY7I9UkFgoksDBBwsBJ6RhQLsZOQMY9Q130_head
{
this:
np:hasAssertion
dgn-np:NP482206.RAFVEsnX12H6jLY7I9UkFgoksDBBwsBJ6RhQLsZOQMY9Q130_assertion
;
np:hasProvenance
dgn-np:NP482206.RAFVEsnX12H6jLY7I9UkFgoksDBBwsBJ6RhQLsZOQMY9Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP482206.RAFVEsnX12H6jLY7I9UkFgoksDBBwsBJ6RhQLsZOQMY9Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP482206.RAFVEsnX12H6jLY7I9UkFgoksDBBwsBJ6RhQLsZOQMY9Q130_assertion
a
np:Assertion
.
dgn-np:NP482206.RAFVEsnX12H6jLY7I9UkFgoksDBBwsBJ6RhQLsZOQMY9Q130_provenance
a
np:Provenance
.
dgn-np:NP482206.RAFVEsnX12H6jLY7I9UkFgoksDBBwsBJ6RhQLsZOQMY9Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP482206.RAFVEsnX12H6jLY7I9UkFgoksDBBwsBJ6RhQLsZOQMY9Q130_assertion
{
miriam-gene:4361
a
ncit:C16612
.
lld:C0043119
a
ncit:C7057
.
dgn-gda:DGN8570b78f1c250bdf60a8c8a748d9567e
sio:SIO_000628
miriam-gene:4361
,
lld:C0043119
;
a
sio:SIO_001121
.
}
dgn-np:NP482206.RAFVEsnX12H6jLY7I9UkFgoksDBBwsBJ6RhQLsZOQMY9Q130_provenance
{
dgn-np:NP482206.RAFVEsnX12H6jLY7I9UkFgoksDBBwsBJ6RhQLsZOQMY9Q130_assertion
dcterms:description
"[Finally, we show that the DNA breakage in replicating cells and apoptosis observed in WS are not enhanced by concomitant knock down of MRE11 by RNAi, indicating that WRN and MRE11 complex act in a common pathway.]. 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:15467456
;
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:NP482206.RAFVEsnX12H6jLY7I9UkFgoksDBBwsBJ6RhQLsZOQMY9Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:48+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" .
}