@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP265736.RA9L-hSPPQe010KmC45OJJkGlM7QUV3KF0ni6R2NHqrmU
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP265736.RA9L-hSPPQe010KmC45OJJkGlM7QUV3KF0ni6R2NHqrmU130_assertion
;
np:hasProvenance
dgn-np:NP265736.RA9L-hSPPQe010KmC45OJJkGlM7QUV3KF0ni6R2NHqrmU130_provenance
;
np:hasPublicationInfo
dgn-np:NP265736.RA9L-hSPPQe010KmC45OJJkGlM7QUV3KF0ni6R2NHqrmU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP265736.RA9L-hSPPQe010KmC45OJJkGlM7QUV3KF0ni6R2NHqrmU130_assertion
a
np:Assertion
.
dgn-np:NP265736.RA9L-hSPPQe010KmC45OJJkGlM7QUV3KF0ni6R2NHqrmU130_provenance
a
np:Provenance
.
dgn-np:NP265736.RA9L-hSPPQe010KmC45OJJkGlM7QUV3KF0ni6R2NHqrmU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP265736.RA9L-hSPPQe010KmC45OJJkGlM7QUV3KF0ni6R2NHqrmU130_assertion
{
miriam-gene:653689
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGN185beaaad2ee17a12ec98d045476a84d
sio:SIO_000628
miriam-gene:653689
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP265736.RA9L-hSPPQe010KmC45OJJkGlM7QUV3KF0ni6R2NHqrmU130_provenance
{
dgn-np:NP265736.RA9L-hSPPQe010KmC45OJJkGlM7QUV3KF0ni6R2NHqrmU130_assertion
dcterms:description
"[We evaluated the influence of the GSTT1 and GSTT2B deletion polymorphisms, and the GSTP1 Ile105Val polymorphism (rs1695) on susceptibility to oesophageal squamous cell carcinoma (OSCC) in the Black and Mixed Ancestry populations of South Africa.]. 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:22216261
;
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:NP265736.RA9L-hSPPQe010KmC45OJJkGlM7QUV3KF0ni6R2NHqrmU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:28+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
<
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" .
}