@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP891358.RAgmahjDKaZN_lDWhvMdiyr1TykJDFdcTnUKw9g1hq7Ns
> .
@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:NP891358.RAgmahjDKaZN_lDWhvMdiyr1TykJDFdcTnUKw9g1hq7Ns130_head
{
this:
np:hasAssertion
dgn-np:NP891358.RAgmahjDKaZN_lDWhvMdiyr1TykJDFdcTnUKw9g1hq7Ns130_assertion
;
np:hasProvenance
dgn-np:NP891358.RAgmahjDKaZN_lDWhvMdiyr1TykJDFdcTnUKw9g1hq7Ns130_provenance
;
np:hasPublicationInfo
dgn-np:NP891358.RAgmahjDKaZN_lDWhvMdiyr1TykJDFdcTnUKw9g1hq7Ns130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP891358.RAgmahjDKaZN_lDWhvMdiyr1TykJDFdcTnUKw9g1hq7Ns130_assertion
a
np:Assertion
.
dgn-np:NP891358.RAgmahjDKaZN_lDWhvMdiyr1TykJDFdcTnUKw9g1hq7Ns130_provenance
a
np:Provenance
.
dgn-np:NP891358.RAgmahjDKaZN_lDWhvMdiyr1TykJDFdcTnUKw9g1hq7Ns130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP891358.RAgmahjDKaZN_lDWhvMdiyr1TykJDFdcTnUKw9g1hq7Ns130_assertion
{
miriam-gene:5961
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN165ce2107ff0d0a8bc7134785d8daba6
sio:SIO_000628
miriam-gene:5961
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP891358.RAgmahjDKaZN_lDWhvMdiyr1TykJDFdcTnUKw9g1hq7Ns130_provenance
{
dgn-np:NP891358.RAgmahjDKaZN_lDWhvMdiyr1TykJDFdcTnUKw9g1hq7Ns130_assertion
dcterms:description
"[Contrasting with the absence of any developmental abnormality, biological analyses revealed defects similar to those observed in NBS patients, including chromosomal instability, cellular hyperradiosensitivity and checkpoint defects as measured by radioresistant DNA synthesis (RDS).]. 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:19105185
;
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:NP891358.RAgmahjDKaZN_lDWhvMdiyr1TykJDFdcTnUKw9g1hq7Ns130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:08+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" .
}