@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP73938.RA-4kmXCR9Dv9TXeHl3zsP0rYLCatpNjANsr_fBoLuD2A
> .
@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:NP73938.RA-4kmXCR9Dv9TXeHl3zsP0rYLCatpNjANsr_fBoLuD2A130_head
{
this:
np:hasAssertion
dgn-np:NP73938.RA-4kmXCR9Dv9TXeHl3zsP0rYLCatpNjANsr_fBoLuD2A130_assertion
;
np:hasProvenance
dgn-np:NP73938.RA-4kmXCR9Dv9TXeHl3zsP0rYLCatpNjANsr_fBoLuD2A130_provenance
;
np:hasPublicationInfo
dgn-np:NP73938.RA-4kmXCR9Dv9TXeHl3zsP0rYLCatpNjANsr_fBoLuD2A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP73938.RA-4kmXCR9Dv9TXeHl3zsP0rYLCatpNjANsr_fBoLuD2A130_assertion
a
np:Assertion
.
dgn-np:NP73938.RA-4kmXCR9Dv9TXeHl3zsP0rYLCatpNjANsr_fBoLuD2A130_provenance
a
np:Provenance
.
dgn-np:NP73938.RA-4kmXCR9Dv9TXeHl3zsP0rYLCatpNjANsr_fBoLuD2A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP73938.RA-4kmXCR9Dv9TXeHl3zsP0rYLCatpNjANsr_fBoLuD2A130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNc60e8f9236d3337f38dca5b170436b97
sio:SIO_000628
miriam-gene:2952
,
lld:C0027651
;
a
sio:SIO_001122
.
}
dgn-np:NP73938.RA-4kmXCR9Dv9TXeHl3zsP0rYLCatpNjANsr_fBoLuD2A130_provenance
{
dgn-np:NP73938.RA-4kmXCR9Dv9TXeHl3zsP0rYLCatpNjANsr_fBoLuD2A130_assertion
dcterms:description
"[The NE Indians differ from the rest of the Indian population with reference to genotypic distribution of GST polymorphisms but the frequency was found to be similar to that which has been reported from China. This may explain the hypothesis of the common ancestral origin of both the NE Indians and the Chinese and a higher frequency of cancers such as gastric, esophageal, and oral cancers, which has been reported from these regions. This study establishes baseline frequency data for GST polymorphisms for future case control studies on the role these polymorphisms play with regard to diseases. The results presented here provide the first report on GST polymorphisms in the NE Indian population.]. 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:20073549
;
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:NP73938.RA-4kmXCR9Dv9TXeHl3zsP0rYLCatpNjANsr_fBoLuD2A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:36+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" .
}