@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP67884.RAq9RF5l4kc3_OaxxdLFClTGQYG9U8WdL1xsVNHYLvgoY
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP67884.RAq9RF5l4kc3_OaxxdLFClTGQYG9U8WdL1xsVNHYLvgoY130_head
{
this:
np:hasAssertion
dgn-np:NP67884.RAq9RF5l4kc3_OaxxdLFClTGQYG9U8WdL1xsVNHYLvgoY130_assertion
;
np:hasProvenance
dgn-np:NP67884.RAq9RF5l4kc3_OaxxdLFClTGQYG9U8WdL1xsVNHYLvgoY130_provenance
;
np:hasPublicationInfo
dgn-np:NP67884.RAq9RF5l4kc3_OaxxdLFClTGQYG9U8WdL1xsVNHYLvgoY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP67884.RAq9RF5l4kc3_OaxxdLFClTGQYG9U8WdL1xsVNHYLvgoY130_assertion
a
np:Assertion
.
dgn-np:NP67884.RAq9RF5l4kc3_OaxxdLFClTGQYG9U8WdL1xsVNHYLvgoY130_provenance
a
np:Provenance
.
dgn-np:NP67884.RAq9RF5l4kc3_OaxxdLFClTGQYG9U8WdL1xsVNHYLvgoY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP67884.RAq9RF5l4kc3_OaxxdLFClTGQYG9U8WdL1xsVNHYLvgoY130_assertion
{
miriam-gene:9
a
ncit:C16612
.
lld:C0004096
a
ncit:C7057
.
dgn-gda:DGN15f3c3ca54173f29e36685d38b2351bf
sio:SIO_000628
miriam-gene:9
,
lld:C0004096
;
a
sio:SIO_001122
.
}
dgn-np:NP67884.RAq9RF5l4kc3_OaxxdLFClTGQYG9U8WdL1xsVNHYLvgoY130_provenance
{
dgn-np:NP67884.RAq9RF5l4kc3_OaxxdLFClTGQYG9U8WdL1xsVNHYLvgoY130_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-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP67884.RAq9RF5l4kc3_OaxxdLFClTGQYG9U8WdL1xsVNHYLvgoY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:17+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}