@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8
> .
@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:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_head
{
this:
np:hasAssertion
dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_assertion
;
np:hasProvenance
dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_provenance
;
np:hasPublicationInfo
dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_assertion
a
np:Assertion
.
dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_provenance
a
np:Provenance
.
dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_assertion
{
miriam-gene:641
a
ncit:C16612
.
lld:C0231341
a
ncit:C7057
.
dgn-gda:DGN034eacb8dcd81b6d7ab5895779d54422
sio:SIO_000628
miriam-gene:641
,
lld:C0231341
;
a
sio:SIO_001121
.
}
dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_provenance
{
dgn-np:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_assertion
dcterms:description
"[Human cells defective in a different RecQ helicase, the WRN protein involved in the premature aging Werner syndrome, do not exhibit the gene cluster instability (GCI) phenotype, indicating that the BLM protein specifically, rather than RecQ helicases generally, holds back this recombination-mediated genomic instability.]. 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:19542097
;
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:NP471763.RAmC7yhfgpSA38A5_RJlUg-IYfc9bvREejf-gGlRNo-g8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:43+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" .
}