@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP714772.RA1v4l2jCJ7IfBrx3hQMspkx1JC77ua94kdD6SHRK0ZeQ
> .
@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:NP714772.RA1v4l2jCJ7IfBrx3hQMspkx1JC77ua94kdD6SHRK0ZeQ130_head
{
this:
np:hasAssertion
dgn-np:NP714772.RA1v4l2jCJ7IfBrx3hQMspkx1JC77ua94kdD6SHRK0ZeQ130_assertion
;
np:hasProvenance
dgn-np:NP714772.RA1v4l2jCJ7IfBrx3hQMspkx1JC77ua94kdD6SHRK0ZeQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP714772.RA1v4l2jCJ7IfBrx3hQMspkx1JC77ua94kdD6SHRK0ZeQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP714772.RA1v4l2jCJ7IfBrx3hQMspkx1JC77ua94kdD6SHRK0ZeQ130_assertion
a
np:Assertion
.
dgn-np:NP714772.RA1v4l2jCJ7IfBrx3hQMspkx1JC77ua94kdD6SHRK0ZeQ130_provenance
a
np:Provenance
.
dgn-np:NP714772.RA1v4l2jCJ7IfBrx3hQMspkx1JC77ua94kdD6SHRK0ZeQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP714772.RA1v4l2jCJ7IfBrx3hQMspkx1JC77ua94kdD6SHRK0ZeQ130_assertion
{
miriam-gene:7517
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN43288b460a8a21a719e812ce6f4012c0
sio:SIO_000628
miriam-gene:7517
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP714772.RA1v4l2jCJ7IfBrx3hQMspkx1JC77ua94kdD6SHRK0ZeQ130_provenance
{
dgn-np:NP714772.RA1v4l2jCJ7IfBrx3hQMspkx1JC77ua94kdD6SHRK0ZeQ130_assertion
dcterms:description
"[Changes in the XRCC3 protein lead to an increase in errors in chromosome segregation due to defects in centrosomes, resulting in aneuploidy and other chromosomal aberrations, such as small increases in telomeres.]. 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:22370935
;
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:NP714772.RA1v4l2jCJ7IfBrx3hQMspkx1JC77ua94kdD6SHRK0ZeQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:14+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" .
}