@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP724221.RA8z44s9dTOfdVH1c1_lv9SmNZaJogTBcaoYa4JOxMr_k
> .
@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:NP724221.RA8z44s9dTOfdVH1c1_lv9SmNZaJogTBcaoYa4JOxMr_k130_head
{
this:
np:hasAssertion
dgn-np:NP724221.RA8z44s9dTOfdVH1c1_lv9SmNZaJogTBcaoYa4JOxMr_k130_assertion
;
np:hasProvenance
dgn-np:NP724221.RA8z44s9dTOfdVH1c1_lv9SmNZaJogTBcaoYa4JOxMr_k130_provenance
;
np:hasPublicationInfo
dgn-np:NP724221.RA8z44s9dTOfdVH1c1_lv9SmNZaJogTBcaoYa4JOxMr_k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP724221.RA8z44s9dTOfdVH1c1_lv9SmNZaJogTBcaoYa4JOxMr_k130_assertion
a
np:Assertion
.
dgn-np:NP724221.RA8z44s9dTOfdVH1c1_lv9SmNZaJogTBcaoYa4JOxMr_k130_provenance
a
np:Provenance
.
dgn-np:NP724221.RA8z44s9dTOfdVH1c1_lv9SmNZaJogTBcaoYa4JOxMr_k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP724221.RA8z44s9dTOfdVH1c1_lv9SmNZaJogTBcaoYa4JOxMr_k130_assertion
{
miriam-gene:145389
a
ncit:C16612
.
lld:C0264423
a
ncit:C7057
.
dgn-gda:DGNd8a1d0489bd300d57ccaccba9d9ef1d9
sio:SIO_000628
miriam-gene:145389
,
lld:C0264423
;
a
sio:SIO_001121
.
}
dgn-np:NP724221.RA8z44s9dTOfdVH1c1_lv9SmNZaJogTBcaoYa4JOxMr_k130_provenance
{
dgn-np:NP724221.RA8z44s9dTOfdVH1c1_lv9SmNZaJogTBcaoYa4JOxMr_k130_assertion
dcterms:description
"[Association studies on NAT1 and NAT2 polymorphisms focused in this review indicate the genetic significance of slow acetylation phenotype in bronchial and occupational asthma as well as in other allergic diseases in different populations worldwide.]. 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:18680475
;
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:NP724221.RA8z44s9dTOfdVH1c1_lv9SmNZaJogTBcaoYa4JOxMr_k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:19+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" .
}