@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc
> .
@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:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_head
{
this:
np:hasAssertion
dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_assertion
;
np:hasProvenance
dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_provenance
;
np:hasPublicationInfo
dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_assertion
a
np:Assertion
.
dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_provenance
a
np:Provenance
.
dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_assertion
{
miriam-gene:5981
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN46c13ab596d6f9bb8e27192f8cdcc949
sio:SIO_000628
miriam-gene:5981
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_provenance
{
dgn-np:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_assertion
dcterms:description
"[The authors devised a genomic polymerase chain reaction-single strand conformational polymorphism assay followed by sequencing and screened the entire RFC coding region for sequence alterations in DNA from 246 leukemia specimens from patients with diverse ethnic variation, 24 at the time of recurrence and the rest at the time of diagnosis.]. 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:14770434
;
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:NP646035.RAVnn0WN7K6blfDVm5VrWxksoBzqyY4VcEW8SD8dsinVc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:29+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" .
}