@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP504255.RAypP77xkducqC3C5Rp01EkANj6jWqG49aIvAi2T27bVQ
> .
@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:NP504255.RAypP77xkducqC3C5Rp01EkANj6jWqG49aIvAi2T27bVQ130_head
{
this:
np:hasAssertion
dgn-np:NP504255.RAypP77xkducqC3C5Rp01EkANj6jWqG49aIvAi2T27bVQ130_assertion
;
np:hasProvenance
dgn-np:NP504255.RAypP77xkducqC3C5Rp01EkANj6jWqG49aIvAi2T27bVQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP504255.RAypP77xkducqC3C5Rp01EkANj6jWqG49aIvAi2T27bVQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP504255.RAypP77xkducqC3C5Rp01EkANj6jWqG49aIvAi2T27bVQ130_assertion
a
np:Assertion
.
dgn-np:NP504255.RAypP77xkducqC3C5Rp01EkANj6jWqG49aIvAi2T27bVQ130_provenance
a
np:Provenance
.
dgn-np:NP504255.RAypP77xkducqC3C5Rp01EkANj6jWqG49aIvAi2T27bVQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP504255.RAypP77xkducqC3C5Rp01EkANj6jWqG49aIvAi2T27bVQ130_assertion
{
miriam-gene:2837
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN42ab77a3658583332751a917743ed2e6
sio:SIO_000628
miriam-gene:2837
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP504255.RAypP77xkducqC3C5Rp01EkANj6jWqG49aIvAi2T27bVQ130_provenance
{
dgn-np:NP504255.RAypP77xkducqC3C5Rp01EkANj6jWqG49aIvAi2T27bVQ130_assertion
dcterms:description
"[To investigate whether inherited variants in genes encoding proteins that repair DSBs by HR modulate acute myeloid leukaemia (AML) risk, we have examined the frequency of two variants in the 5' untranslated region (UTR) of RAD51 (RAD51 135 G>C and the RAD51 172 G>T) in a large case-control study of acute myeloid leukaemia (AML).]. 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:16890287
;
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:NP504255.RAypP77xkducqC3C5Rp01EkANj6jWqG49aIvAi2T27bVQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}