@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP749409.RADZj4uujF1EMmurG4Rr-trDMGOF1BrR6By1eHtRkuFlE
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP749409.RADZj4uujF1EMmurG4Rr-trDMGOF1BrR6By1eHtRkuFlE130_assertion
;
np:hasProvenance
dgn-np:NP749409.RADZj4uujF1EMmurG4Rr-trDMGOF1BrR6By1eHtRkuFlE130_provenance
;
np:hasPublicationInfo
dgn-np:NP749409.RADZj4uujF1EMmurG4Rr-trDMGOF1BrR6By1eHtRkuFlE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP749409.RADZj4uujF1EMmurG4Rr-trDMGOF1BrR6By1eHtRkuFlE130_assertion
a
np:Assertion
.
dgn-np:NP749409.RADZj4uujF1EMmurG4Rr-trDMGOF1BrR6By1eHtRkuFlE130_provenance
a
np:Provenance
.
dgn-np:NP749409.RADZj4uujF1EMmurG4Rr-trDMGOF1BrR6By1eHtRkuFlE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP749409.RADZj4uujF1EMmurG4Rr-trDMGOF1BrR6By1eHtRkuFlE130_assertion
{
miriam-gene:10
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGNff6ce99add4872552304d88e2f6bb394
sio:SIO_000628
miriam-gene:10
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP749409.RADZj4uujF1EMmurG4Rr-trDMGOF1BrR6By1eHtRkuFlE130_provenance
{
dgn-np:NP749409.RADZj4uujF1EMmurG4Rr-trDMGOF1BrR6By1eHtRkuFlE130_assertion
dcterms:description
"[Our findings do not provide a genetic basis for any association of NIDDM and NAT2 polymorphism, suggesting that any excess of subjects with the rapid acetylator phenotype among patients with NIDDM should be secondary to the disease or concomitant drug therapy.]. 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:8946479
;
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:NP749409.RADZj4uujF1EMmurG4Rr-trDMGOF1BrR6By1eHtRkuFlE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:34+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" .
}