@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI
> .
@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:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_head
{
this:
np:hasAssertion
dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_assertion
;
np:hasProvenance
dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_provenance
;
np:hasPublicationInfo
dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_assertion
a
np:Assertion
.
dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_provenance
a
np:Provenance
.
dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_assertion
{
miriam-gene:10
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN73c7820289948eb56857d33dae65d311
sio:SIO_000628
miriam-gene:10
,
lld:C0004096
;
a
sio:SIO_001122
.
}
dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_provenance
{
dgn-np:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_assertion
dcterms:description
"[Statistically significant increases in asthma risk were also observed among the whole study population for the concurrent presence of the GSTM1 null genotype and either NAT1 (odds ratio OR 4.53, 95% CI 1.76 to 11.6) or NAT2 (OR 3.12, 95% CI 1.11 to 8.78) slow acetylator genotypes, and of NAT1 and NAT2 slow acetylator genotypes (OR 4.20, 95% CI 1.51 to 11.6).]. 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:11927838
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP54027.RAcw4n8HAyl3f-ijVJHpBDzlpM23pU2QZoCOkDww85qiI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}