@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM
> .
@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:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_head
{
this:
np:hasAssertion
dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_assertion
;
np:hasProvenance
dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_provenance
;
np:hasPublicationInfo
dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_assertion
a
np:Assertion
.
dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_provenance
a
np:Provenance
.
dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_assertion
{
miriam-gene:1161
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN051ef6478097c04b73943d6452a396fa
sio:SIO_000628
miriam-gene:1161
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_provenance
{
dgn-np:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_assertion
dcterms:description
"[We report here cancer risk for cytogenetically tested, healthy subjects with respect to frequency of CAs, CSAs, and CTAs in peripheral blood lymphocytes, using Nordic (1981 subjects with CA data, 1871 subjects with CSA/CTA data) and Italian (1573 subjects with CA data, 877 subjects with CTA/CSA data) cohorts, with a median follow-up of 17 years.]. 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:15026371
;
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:NP918034.RA0tPUpaeDAEv3BppoOZWCDmtPjqGBuQv7BB7Fd6lr5jM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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" .
}