@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP54246.RAIAQq3XmMk_mMGXfdxM-_l8Vne0zlQMbr_utmFO7auMU
> .
@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:NP54246.RAIAQq3XmMk_mMGXfdxM-_l8Vne0zlQMbr_utmFO7auMU130_head
{
this:
np:hasAssertion
dgn-np:NP54246.RAIAQq3XmMk_mMGXfdxM-_l8Vne0zlQMbr_utmFO7auMU130_assertion
;
np:hasProvenance
dgn-np:NP54246.RAIAQq3XmMk_mMGXfdxM-_l8Vne0zlQMbr_utmFO7auMU130_provenance
;
np:hasPublicationInfo
dgn-np:NP54246.RAIAQq3XmMk_mMGXfdxM-_l8Vne0zlQMbr_utmFO7auMU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP54246.RAIAQq3XmMk_mMGXfdxM-_l8Vne0zlQMbr_utmFO7auMU130_assertion
a
np:Assertion
.
dgn-np:NP54246.RAIAQq3XmMk_mMGXfdxM-_l8Vne0zlQMbr_utmFO7auMU130_provenance
a
np:Provenance
.
dgn-np:NP54246.RAIAQq3XmMk_mMGXfdxM-_l8Vne0zlQMbr_utmFO7auMU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP54246.RAIAQq3XmMk_mMGXfdxM-_l8Vne0zlQMbr_utmFO7auMU130_assertion
{
miriam-gene:4552
a
ncit:C16612
.
lld:C0598309
a
ncit:C7057
.
dgn-gda:DGN6a55dbb3425fdf97cf6d9d8ea8b376a3
sio:SIO_000628
miriam-gene:4552
,
lld:C0598309
;
a
sio:SIO_001122
.
}
dgn-np:NP54246.RAIAQq3XmMk_mMGXfdxM-_l8Vne0zlQMbr_utmFO7auMU130_provenance
{
dgn-np:NP54246.RAIAQq3XmMk_mMGXfdxM-_l8Vne0zlQMbr_utmFO7auMU130_assertion
dcterms:description
"[Overall, the results obtained suggest that both folate status and relevant metabolic genotype can influence background levels of DNA damage in normal subjects. The significant association observed in smokers between plasma vitamin B12 and SCE frequencies may highlight the effect of methylation status on DNA damage and repair, although the role of other, unidentified dietary factors cannot be ruled out. At the same time, micronucleus data indicate that the MTRR 66GG variant may represent another individual trait of relative genomic instability, thus supporting epidemiological data on increased risk of Down syndrome conception in MTRR 66GG subjects.]. 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:12807760
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP54246.RAIAQq3XmMk_mMGXfdxM-_l8Vne0zlQMbr_utmFO7auMU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}