@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY
> .
@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:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_head
{
this:
np:hasAssertion
dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_assertion
;
np:hasProvenance
dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_provenance
;
np:hasPublicationInfo
dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_assertion
a
np:Assertion
.
dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_provenance
a
np:Provenance
.
dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_assertion
{
miriam-gene:7521
a
ncit:C16612
.
lld:C0004135
a
ncit:C7057
.
dgn-gda:DGNb8c9bede9c67219361e36810debc8757
sio:SIO_000628
miriam-gene:7521
,
lld:C0004135
;
a
sio:SIO_001121
.
}
dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_provenance
{
dgn-np:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_assertion
dcterms:description
"[In search of functions involved in the regulation of gene amplification, and given the relevance of chromosome breakage in initiating the process, we analyzed the gene amplification ability of cells hypersensitive to inducers of DNA double-strand breaks and defective in cell cycle control: two human fibroblast strains derived from patients affected by ataxia telangiectasia (AT) and two hamster mutant cell lines belonging to complementation group XRCC8 of the rodent X-ray-sensitive mutants.]. 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:11159752
;
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:NP774927.RA2cWqTWYtf_OEEylfnKJrClJ5M05yf1aUkP9gdzzBkaY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:48+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" .
}