@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY
> .
@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:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_head
{
this:
np:hasAssertion
dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_assertion
;
np:hasProvenance
dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_provenance
;
np:hasPublicationInfo
dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_assertion
a
np:Assertion
.
dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_provenance
a
np:Provenance
.
dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_assertion
{
miriam-gene:133482
a
ncit:C16612
.
lld:C0007115
a
ncit:C7057
.
dgn-gda:DGN49c5886d89dc8864c5412caa4670ec7f
sio:SIO_000628
miriam-gene:133482
,
lld:C0007115
;
a
sio:SIO_001121
.
}
dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_provenance
{
dgn-np:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_assertion
dcterms:description
"[Nevertheless, as far as we know, only few studies have been conducted linking thyroid cancer incidence and GST polymorphisms, and no data are available on the possible association between NAT2 polymorphisms and thyroid cancer risk.]. 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:19169061
;
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:NP762587.RAXHkcfyVc3LdskypK8V34EKOybcLxVtop0eDbEap1pmY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:41+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" .
}