@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP617736.RARhDVFOpMdRKhdx2jUD00Kus481esIhOFHN2IFHaXGfM
> .
@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:NP617736.RARhDVFOpMdRKhdx2jUD00Kus481esIhOFHN2IFHaXGfM130_head
{
this:
np:hasAssertion
dgn-np:NP617736.RARhDVFOpMdRKhdx2jUD00Kus481esIhOFHN2IFHaXGfM130_assertion
;
np:hasProvenance
dgn-np:NP617736.RARhDVFOpMdRKhdx2jUD00Kus481esIhOFHN2IFHaXGfM130_provenance
;
np:hasPublicationInfo
dgn-np:NP617736.RARhDVFOpMdRKhdx2jUD00Kus481esIhOFHN2IFHaXGfM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP617736.RARhDVFOpMdRKhdx2jUD00Kus481esIhOFHN2IFHaXGfM130_assertion
a
np:Assertion
.
dgn-np:NP617736.RARhDVFOpMdRKhdx2jUD00Kus481esIhOFHN2IFHaXGfM130_provenance
a
np:Provenance
.
dgn-np:NP617736.RARhDVFOpMdRKhdx2jUD00Kus481esIhOFHN2IFHaXGfM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP617736.RARhDVFOpMdRKhdx2jUD00Kus481esIhOFHN2IFHaXGfM130_assertion
{
miriam-gene:1540
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN0bfec4e342640dd8c61c7fcb5d899c68
sio:SIO_000628
miriam-gene:1540
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP617736.RARhDVFOpMdRKhdx2jUD00Kus481esIhOFHN2IFHaXGfM130_provenance
{
dgn-np:NP617736.RARhDVFOpMdRKhdx2jUD00Kus481esIhOFHN2IFHaXGfM130_assertion
dcterms:description
"[Variant frequencies of the Nø, Mø, and MM cell types in atomic bomb survivors determined by SBS measurements were found to increase with radiation dose (DS86, kerma) as well as with the frequency of chromosome aberrations in lymphocytes.]. 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:2910480
;
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:NP617736.RARhDVFOpMdRKhdx2jUD00Kus481esIhOFHN2IFHaXGfM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:13+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" .
}