@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM
> .
@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:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_head
{
this:
np:hasAssertion
dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_assertion
;
np:hasProvenance
dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_provenance
;
np:hasPublicationInfo
dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_assertion
a
np:Assertion
.
dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_provenance
a
np:Provenance
.
dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_assertion
{
miriam-gene:3014
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN132d3524df95bed4f9d85070377d79f9
sio:SIO_000628
miriam-gene:3014
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_provenance
{
dgn-np:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_assertion
dcterms:description
"[The systematic study of DDR in human tumors and normal tissues by high-throughput tissue microarrays revealed that ATM and gamma-H2AX were engaged in cancer but the extent of their activation was strongly affected by the organ and cell type involved, whereas 53BP1 loss was the most consistent feature among the tumor studied.]. 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:17522062
;
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:NP671308.RAnPltJa95TfTdK2HLJSbclPG73Ezi_4WlFvpJ59KrTyM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}