@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP824476.RAxqclrZxmN3lpyS7b5wwUFkk5ZT9Zqfu22kssLOsBavc
> .
@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:NP824476.RAxqclrZxmN3lpyS7b5wwUFkk5ZT9Zqfu22kssLOsBavc130_head
{
this:
np:hasAssertion
dgn-np:NP824476.RAxqclrZxmN3lpyS7b5wwUFkk5ZT9Zqfu22kssLOsBavc130_assertion
;
np:hasProvenance
dgn-np:NP824476.RAxqclrZxmN3lpyS7b5wwUFkk5ZT9Zqfu22kssLOsBavc130_provenance
;
np:hasPublicationInfo
dgn-np:NP824476.RAxqclrZxmN3lpyS7b5wwUFkk5ZT9Zqfu22kssLOsBavc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP824476.RAxqclrZxmN3lpyS7b5wwUFkk5ZT9Zqfu22kssLOsBavc130_assertion
a
np:Assertion
.
dgn-np:NP824476.RAxqclrZxmN3lpyS7b5wwUFkk5ZT9Zqfu22kssLOsBavc130_provenance
a
np:Provenance
.
dgn-np:NP824476.RAxqclrZxmN3lpyS7b5wwUFkk5ZT9Zqfu22kssLOsBavc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP824476.RAxqclrZxmN3lpyS7b5wwUFkk5ZT9Zqfu22kssLOsBavc130_assertion
{
miriam-gene:780
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGN5bd90501a6fd0d2f28038866b455cbcd
sio:SIO_000628
miriam-gene:780
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP824476.RAxqclrZxmN3lpyS7b5wwUFkk5ZT9Zqfu22kssLOsBavc130_provenance
{
dgn-np:NP824476.RAxqclrZxmN3lpyS7b5wwUFkk5ZT9Zqfu22kssLOsBavc130_assertion
dcterms:description
"[In conclusion, we demonstrate the heterogeneity of the DDR response in MDS and AML and provide evidence for its selective suppression in AML because of the uncoupling between activated ATM and inactive checkpoint kinases.]. 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:19398952
;
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:NP824476.RAxqclrZxmN3lpyS7b5wwUFkk5ZT9Zqfu22kssLOsBavc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:25+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" .
}