@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP676529.RAk1ofVITO-20ELbMnvE6LNSA7mtyAi4UiYNSZJTPvmjM
> .
@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:NP676529.RAk1ofVITO-20ELbMnvE6LNSA7mtyAi4UiYNSZJTPvmjM130_head
{
this:
np:hasAssertion
dgn-np:NP676529.RAk1ofVITO-20ELbMnvE6LNSA7mtyAi4UiYNSZJTPvmjM130_assertion
;
np:hasProvenance
dgn-np:NP676529.RAk1ofVITO-20ELbMnvE6LNSA7mtyAi4UiYNSZJTPvmjM130_provenance
;
np:hasPublicationInfo
dgn-np:NP676529.RAk1ofVITO-20ELbMnvE6LNSA7mtyAi4UiYNSZJTPvmjM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP676529.RAk1ofVITO-20ELbMnvE6LNSA7mtyAi4UiYNSZJTPvmjM130_assertion
a
np:Assertion
.
dgn-np:NP676529.RAk1ofVITO-20ELbMnvE6LNSA7mtyAi4UiYNSZJTPvmjM130_provenance
a
np:Provenance
.
dgn-np:NP676529.RAk1ofVITO-20ELbMnvE6LNSA7mtyAi4UiYNSZJTPvmjM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP676529.RAk1ofVITO-20ELbMnvE6LNSA7mtyAi4UiYNSZJTPvmjM130_assertion
{
miriam-gene:6046
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN987c16277e62b55c2a61a937dc2888a0
sio:SIO_000628
miriam-gene:6046
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP676529.RAk1ofVITO-20ELbMnvE6LNSA7mtyAi4UiYNSZJTPvmjM130_provenance
{
dgn-np:NP676529.RAk1ofVITO-20ELbMnvE6LNSA7mtyAi4UiYNSZJTPvmjM130_assertion
dcterms:description
"[Since polymorphic variants in the glutathione S-transferase (GST) and N-acetyl transferase (NAT) genes have been associated with cancer risk, we explored the possible links between GSTM1, GSTP1, GSTT1 and NAT2 variants and the frequency of micronuclei (MN) in human 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:16621679
;
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:NP676529.RAk1ofVITO-20ELbMnvE6LNSA7mtyAi4UiYNSZJTPvmjM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:48+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" .
}