@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1322997.RAN0EltIksumb7zdRpLTPZETjf-WPpcOpduhbRi3oUKVg
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1322997.RAN0EltIksumb7zdRpLTPZETjf-WPpcOpduhbRi3oUKVg130_head
{
this:
np:hasAssertion
dgn-np:NP1322997.RAN0EltIksumb7zdRpLTPZETjf-WPpcOpduhbRi3oUKVg130_assertion
;
np:hasProvenance
dgn-np:NP1322997.RAN0EltIksumb7zdRpLTPZETjf-WPpcOpduhbRi3oUKVg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1322997.RAN0EltIksumb7zdRpLTPZETjf-WPpcOpduhbRi3oUKVg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1322997.RAN0EltIksumb7zdRpLTPZETjf-WPpcOpduhbRi3oUKVg130_assertion
a
np:Assertion
.
dgn-np:NP1322997.RAN0EltIksumb7zdRpLTPZETjf-WPpcOpduhbRi3oUKVg130_provenance
a
np:Provenance
.
dgn-np:NP1322997.RAN0EltIksumb7zdRpLTPZETjf-WPpcOpduhbRi3oUKVg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1322997.RAN0EltIksumb7zdRpLTPZETjf-WPpcOpduhbRi3oUKVg130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0005859
a
ncit:C7057
.
dgn-gda:DGN50ac3b803bf58338bb0a83ba5c757909
sio:SIO_000628
miriam-gene:7157
,
lld:C0005859
;
a
sio:SIO_001121
.
}
dgn-np:NP1322997.RAN0EltIksumb7zdRpLTPZETjf-WPpcOpduhbRi3oUKVg130_provenance
{
dgn-np:NP1322997.RAN0EltIksumb7zdRpLTPZETjf-WPpcOpduhbRi3oUKVg130_assertion
dcterms:description
"[These observations are in line with recent reports showing that at least certain cell lines from other chromosome breakage syndromes, such as ataxia telangiectasia and Bloom syndrome, may be also defective for radiation-induced increase of p53 protein.]. 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:7824283
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1322997.RAN0EltIksumb7zdRpLTPZETjf-WPpcOpduhbRi3oUKVg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:46+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}