@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP6710.RAD3VosyfqxU7vFLLFCjQzS1dsq_sDD3O78BS8wjImMe0
> .
@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 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:NP6710.RAD3VosyfqxU7vFLLFCjQzS1dsq_sDD3O78BS8wjImMe0130_head
{
this:
np:hasAssertion
dgn-np:NP6710.RAD3VosyfqxU7vFLLFCjQzS1dsq_sDD3O78BS8wjImMe0130_assertion
;
np:hasProvenance
dgn-np:NP6710.RAD3VosyfqxU7vFLLFCjQzS1dsq_sDD3O78BS8wjImMe0130_provenance
;
np:hasPublicationInfo
dgn-np:NP6710.RAD3VosyfqxU7vFLLFCjQzS1dsq_sDD3O78BS8wjImMe0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP6710.RAD3VosyfqxU7vFLLFCjQzS1dsq_sDD3O78BS8wjImMe0130_assertion
a
np:Assertion
.
dgn-np:NP6710.RAD3VosyfqxU7vFLLFCjQzS1dsq_sDD3O78BS8wjImMe0130_provenance
a
np:Provenance
.
dgn-np:NP6710.RAD3VosyfqxU7vFLLFCjQzS1dsq_sDD3O78BS8wjImMe0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP6710.RAD3VosyfqxU7vFLLFCjQzS1dsq_sDD3O78BS8wjImMe0130_assertion
{
miriam-gene:7172
a
ncit:C16612
.
lld:C0342801
a
ncit:C7057
.
dgn-gda:DGNbfb8aca98e84ef0e6807252598b68277
sio:SIO_000628
miriam-gene:7172
,
lld:C0342801
;
a
sio:SIO_001122
.
}
dgn-np:NP6710.RAD3VosyfqxU7vFLLFCjQzS1dsq_sDD3O78BS8wjImMe0130_provenance
{
dgn-np:NP6710.RAD3VosyfqxU7vFLLFCjQzS1dsq_sDD3O78BS8wjImMe0130_assertion
dcterms:description
"[This study was designed to investigate in the Sardinian population the frequency distribution of four of the most common variants accounting for TPMT deficiency and to conduct comparative analyses with other populations in order to obtain insights into the main factors that have shaped diversity at the TPMT locus in Sardinia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:16789994
;
prov:wasDerivedFrom
dgn-void:uniprot-20130724
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
dgn-void:uniprot-20130724
pav:importedOn
"2013-07-24"^^
xsd:date
.
}
dgn-np:NP6710.RAD3VosyfqxU7vFLLFCjQzS1dsq_sDD3O78BS8wjImMe0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:01+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" .
}