@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA
> .
@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:NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_head
{
this:
np:hasAssertion
dgn-np:NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_assertion
;
np:hasProvenance
dgn-np:NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance
;
np:hasPublicationInfo
dgn-np:NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_assertion
a
np:Assertion
.
dgn-np:NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance
a
np:Provenance
.
dgn-np:NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_assertion
{
miriam-gene:7517
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN2fe0494cd46e681a793e991b0e100559
sio:SIO_000628
miriam-gene:7517
,
lld:C0023418
;
a
sio:SIO_001122
.
}
dgn-np:NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_provenance
{
dgn-np:NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_assertion
dcterms:description
"[The results indicated that the genotype ratio of NQO1C(609T), RAD51(G135C) and XRCC3(C241T) in single genotype analysis showed no statistical difference between ALL patients and normal controls, which suggested that the single genotype affect onset of ALL without statistical significance.]. 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:19549356
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP59479.RAXEfcld5hoBLmwu53CxToaJSu6-N4xc3FwzIjABmOtmA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:28+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" .
}