@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP748493.RA8hIa2MVfCAL7EtrgqnK0QaZVimd99d6nsnCwiskof4c
> .
@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:NP748493.RA8hIa2MVfCAL7EtrgqnK0QaZVimd99d6nsnCwiskof4c130_head
{
this:
np:hasAssertion
dgn-np:NP748493.RA8hIa2MVfCAL7EtrgqnK0QaZVimd99d6nsnCwiskof4c130_assertion
;
np:hasProvenance
dgn-np:NP748493.RA8hIa2MVfCAL7EtrgqnK0QaZVimd99d6nsnCwiskof4c130_provenance
;
np:hasPublicationInfo
dgn-np:NP748493.RA8hIa2MVfCAL7EtrgqnK0QaZVimd99d6nsnCwiskof4c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP748493.RA8hIa2MVfCAL7EtrgqnK0QaZVimd99d6nsnCwiskof4c130_assertion
a
np:Assertion
.
dgn-np:NP748493.RA8hIa2MVfCAL7EtrgqnK0QaZVimd99d6nsnCwiskof4c130_provenance
a
np:Provenance
.
dgn-np:NP748493.RA8hIa2MVfCAL7EtrgqnK0QaZVimd99d6nsnCwiskof4c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP748493.RA8hIa2MVfCAL7EtrgqnK0QaZVimd99d6nsnCwiskof4c130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0023532
a
ncit:C7057
.
dgn-gda:DGNc4c3b9649b6e7e02ef23292c07767215
sio:SIO_000628
miriam-gene:2952
,
lld:C0023532
;
a
sio:SIO_001121
.
}
dgn-np:NP748493.RA8hIa2MVfCAL7EtrgqnK0QaZVimd99d6nsnCwiskof4c130_provenance
{
dgn-np:NP748493.RA8hIa2MVfCAL7EtrgqnK0QaZVimd99d6nsnCwiskof4c130_assertion
dcterms:description
"[Considering that tobacco is the main etiological factor in oral cancer and that oral leukoplakia is the most prevalent potentially malignant lesion, together with the fact that GSTT1 polymorphism increases the risk of oral squamous cell carcinoma, the purpose of this study was to investigate the GSTT1 null polymorphism and the risk of oral leukoplakia in individuals with tobacco smoking habits in a Brazilian 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:16475728
;
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:NP748493.RA8hIa2MVfCAL7EtrgqnK0QaZVimd99d6nsnCwiskof4c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:33+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" .
}