@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP911084.RAQy8V4adx3BJnxl5XHvlLHIajwidMQX0cSQFH7c61Xf4
> .
@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:NP911084.RAQy8V4adx3BJnxl5XHvlLHIajwidMQX0cSQFH7c61Xf4130_head
{
this:
np:hasAssertion
dgn-np:NP911084.RAQy8V4adx3BJnxl5XHvlLHIajwidMQX0cSQFH7c61Xf4130_assertion
;
np:hasProvenance
dgn-np:NP911084.RAQy8V4adx3BJnxl5XHvlLHIajwidMQX0cSQFH7c61Xf4130_provenance
;
np:hasPublicationInfo
dgn-np:NP911084.RAQy8V4adx3BJnxl5XHvlLHIajwidMQX0cSQFH7c61Xf4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP911084.RAQy8V4adx3BJnxl5XHvlLHIajwidMQX0cSQFH7c61Xf4130_assertion
a
np:Assertion
.
dgn-np:NP911084.RAQy8V4adx3BJnxl5XHvlLHIajwidMQX0cSQFH7c61Xf4130_provenance
a
np:Provenance
.
dgn-np:NP911084.RAQy8V4adx3BJnxl5XHvlLHIajwidMQX0cSQFH7c61Xf4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP911084.RAQy8V4adx3BJnxl5XHvlLHIajwidMQX0cSQFH7c61Xf4130_assertion
{
miriam-gene:256933
a
ncit:C16612
.
lld:C0206695
a
ncit:C7057
.
dgn-gda:DGNae6c735dca86a892085eb73da389e551
sio:SIO_000628
miriam-gene:256933
,
lld:C0206695
;
a
sio:SIO_001121
.
}
dgn-np:NP911084.RAQy8V4adx3BJnxl5XHvlLHIajwidMQX0cSQFH7c61Xf4130_provenance
{
dgn-np:NP911084.RAQy8V4adx3BJnxl5XHvlLHIajwidMQX0cSQFH7c61Xf4130_assertion
dcterms:description
"[The results showed that 30 nM FA was associated with increased frequencies of micronucleated binucleated cell (MNed BNC), nucleoplasmic bridges (NPB), nuclear buds (BUD), apoptosis (APO) and necrosis (NEC) relative to 120 and 240 nM FA (P<0.001) in lymphocytes of case and control groups in vitro, however there were no significant differences between the 120 and 240 nM FA within each sampling group.]. 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:16339195
;
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:NP911084.RAQy8V4adx3BJnxl5XHvlLHIajwidMQX0cSQFH7c61Xf4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:19+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" .
}