@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP927270.RALRRpnBEOKOEeWICp8Jq6bZ9nIeul-MthaFl8G5JcnNE
> .
@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:NP927270.RALRRpnBEOKOEeWICp8Jq6bZ9nIeul-MthaFl8G5JcnNE130_head
{
this:
np:hasAssertion
dgn-np:NP927270.RALRRpnBEOKOEeWICp8Jq6bZ9nIeul-MthaFl8G5JcnNE130_assertion
;
np:hasProvenance
dgn-np:NP927270.RALRRpnBEOKOEeWICp8Jq6bZ9nIeul-MthaFl8G5JcnNE130_provenance
;
np:hasPublicationInfo
dgn-np:NP927270.RALRRpnBEOKOEeWICp8Jq6bZ9nIeul-MthaFl8G5JcnNE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP927270.RALRRpnBEOKOEeWICp8Jq6bZ9nIeul-MthaFl8G5JcnNE130_assertion
a
np:Assertion
.
dgn-np:NP927270.RALRRpnBEOKOEeWICp8Jq6bZ9nIeul-MthaFl8G5JcnNE130_provenance
a
np:Provenance
.
dgn-np:NP927270.RALRRpnBEOKOEeWICp8Jq6bZ9nIeul-MthaFl8G5JcnNE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP927270.RALRRpnBEOKOEeWICp8Jq6bZ9nIeul-MthaFl8G5JcnNE130_assertion
{
miriam-gene:1443
a
ncit:C16612
.
lld:C0008626
a
ncit:C7057
.
dgn-gda:DGN0e994b9a8cc6dd4852ea41b0b6b287ca
sio:SIO_000628
miriam-gene:1443
,
lld:C0008626
;
a
sio:SIO_001121
.
}
dgn-np:NP927270.RALRRpnBEOKOEeWICp8Jq6bZ9nIeul-MthaFl8G5JcnNE130_provenance
{
dgn-np:NP927270.RALRRpnBEOKOEeWICp8Jq6bZ9nIeul-MthaFl8G5JcnNE130_assertion
dcterms:description
"[We have studied the effect of genetic polymorphisms in the DNA repair genes hOGG1, XRCC1, XRCC3, ERCC2 and the MTHFR gene in the folate metabolism on the frequencies of cells with chromosomal aberrations (CA), chromosome-type aberrations (CSA), chromatid-type aberrations (CTA), chromatid breaks (CTB) and chromatid gaps (CTG) scored in peripheral blood lymphocytes from 651 Norwegian subjects of Caucasian descendant.]. 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:16997330
;
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:NP927270.RALRRpnBEOKOEeWICp8Jq6bZ9nIeul-MthaFl8G5JcnNE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:28+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
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" .
}