@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP217144.RAao43_SuP0egrlftnyY0mEzVw2yA_7LQ-zT4elczHVTg
> .
@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:NP217144.RAao43_SuP0egrlftnyY0mEzVw2yA_7LQ-zT4elczHVTg130_head
{
this:
np:hasAssertion
dgn-np:NP217144.RAao43_SuP0egrlftnyY0mEzVw2yA_7LQ-zT4elczHVTg130_assertion
;
np:hasProvenance
dgn-np:NP217144.RAao43_SuP0egrlftnyY0mEzVw2yA_7LQ-zT4elczHVTg130_provenance
;
np:hasPublicationInfo
dgn-np:NP217144.RAao43_SuP0egrlftnyY0mEzVw2yA_7LQ-zT4elczHVTg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP217144.RAao43_SuP0egrlftnyY0mEzVw2yA_7LQ-zT4elczHVTg130_assertion
a
np:Assertion
.
dgn-np:NP217144.RAao43_SuP0egrlftnyY0mEzVw2yA_7LQ-zT4elczHVTg130_provenance
a
np:Provenance
.
dgn-np:NP217144.RAao43_SuP0egrlftnyY0mEzVw2yA_7LQ-zT4elczHVTg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP217144.RAao43_SuP0egrlftnyY0mEzVw2yA_7LQ-zT4elczHVTg130_assertion
{
miriam-gene:2944
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN24eb992c9c0cc1a8489a8b4c0a3a787e
sio:SIO_000628
miriam-gene:2944
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP217144.RAao43_SuP0egrlftnyY0mEzVw2yA_7LQ-zT4elczHVTg130_provenance
{
dgn-np:NP217144.RAao43_SuP0egrlftnyY0mEzVw2yA_7LQ-zT4elczHVTg130_assertion
dcterms:description
"[With the large population in this study, we believed that our results are reliable estimates of the frequencies of the polymorphic CYP2E1 and GSTM1 alleles in Thai population and should provide a base for further epidemiological studies on their links with cancer development.]. 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:17059334
;
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:NP217144.RAao43_SuP0egrlftnyY0mEzVw2yA_7LQ-zT4elczHVTg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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
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"v2.1.0" .
}