@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP933738.RAhHB4fCmAep9FDk1eW1GfNc_kMEB_Fy_22dA7XHuQ-RI
> .
@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:NP933738.RAhHB4fCmAep9FDk1eW1GfNc_kMEB_Fy_22dA7XHuQ-RI130_head
{
this:
np:hasAssertion
dgn-np:NP933738.RAhHB4fCmAep9FDk1eW1GfNc_kMEB_Fy_22dA7XHuQ-RI130_assertion
;
np:hasProvenance
dgn-np:NP933738.RAhHB4fCmAep9FDk1eW1GfNc_kMEB_Fy_22dA7XHuQ-RI130_provenance
;
np:hasPublicationInfo
dgn-np:NP933738.RAhHB4fCmAep9FDk1eW1GfNc_kMEB_Fy_22dA7XHuQ-RI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP933738.RAhHB4fCmAep9FDk1eW1GfNc_kMEB_Fy_22dA7XHuQ-RI130_assertion
a
np:Assertion
.
dgn-np:NP933738.RAhHB4fCmAep9FDk1eW1GfNc_kMEB_Fy_22dA7XHuQ-RI130_provenance
a
np:Provenance
.
dgn-np:NP933738.RAhHB4fCmAep9FDk1eW1GfNc_kMEB_Fy_22dA7XHuQ-RI130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:133482
a
ncit:C16612
.
lld:C0278996
a
ncit:C7057
.
dgn-gda:DGNf723c463183a44d1fa8399e4bf6e57d3
sio:SIO_000628
miriam-gene:133482
,
lld:C0278996
;
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.
}
dgn-np:NP933738.RAhHB4fCmAep9FDk1eW1GfNc_kMEB_Fy_22dA7XHuQ-RI130_provenance
{
dgn-np:NP933738.RAhHB4fCmAep9FDk1eW1GfNc_kMEB_Fy_22dA7XHuQ-RI130_assertion
dcterms:description
"[In conclusion, both the meta- and pooled analysis support modest associations of GSTM1 and GSTT1 genotypes with head and neck cancer risk, and our pooled analysis supports the notion of greater risk when genotypes at multiple GST loci are considered in a multigenic model.]. 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:14693745
;
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:NP933738.RAhHB4fCmAep9FDk1eW1GfNc_kMEB_Fy_22dA7XHuQ-RI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:32+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
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"v2.1.0" .
}