@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP695654.RAc1p9yHpTsHB2Xy6MVJUN3ASX9HsnHuxrAMHamSrG_Hw
> .
@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:NP695654.RAc1p9yHpTsHB2Xy6MVJUN3ASX9HsnHuxrAMHamSrG_Hw130_head
{
this:
np:hasAssertion
dgn-np:NP695654.RAc1p9yHpTsHB2Xy6MVJUN3ASX9HsnHuxrAMHamSrG_Hw130_assertion
;
np:hasProvenance
dgn-np:NP695654.RAc1p9yHpTsHB2Xy6MVJUN3ASX9HsnHuxrAMHamSrG_Hw130_provenance
;
np:hasPublicationInfo
dgn-np:NP695654.RAc1p9yHpTsHB2Xy6MVJUN3ASX9HsnHuxrAMHamSrG_Hw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP695654.RAc1p9yHpTsHB2Xy6MVJUN3ASX9HsnHuxrAMHamSrG_Hw130_assertion
a
np:Assertion
.
dgn-np:NP695654.RAc1p9yHpTsHB2Xy6MVJUN3ASX9HsnHuxrAMHamSrG_Hw130_provenance
a
np:Provenance
.
dgn-np:NP695654.RAc1p9yHpTsHB2Xy6MVJUN3ASX9HsnHuxrAMHamSrG_Hw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP695654.RAc1p9yHpTsHB2Xy6MVJUN3ASX9HsnHuxrAMHamSrG_Hw130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0035243
a
ncit:C7057
.
dgn-gda:DGNb30b4d8d6d3946412739f1a740c12167
sio:SIO_000628
miriam-gene:4360
,
lld:C0035243
;
a
sio:SIO_001121
.
}
dgn-np:NP695654.RAc1p9yHpTsHB2Xy6MVJUN3ASX9HsnHuxrAMHamSrG_Hw130_provenance
{
dgn-np:NP695654.RAc1p9yHpTsHB2Xy6MVJUN3ASX9HsnHuxrAMHamSrG_Hw130_assertion
dcterms:description
"[We used the same collection of isolates to explore the role of hypermutation in this process, since one of the hallmarks of CRI is the high prevalence of DNA mismatch repair (MMR) system-deficient mutator strains.]. 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:18849421
;
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:NP695654.RAc1p9yHpTsHB2Xy6MVJUN3ASX9HsnHuxrAMHamSrG_Hw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:03+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" .
}