@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP129499.RA88rz_2gl0WsS0Ot_Qachqgi7ZXnNZeTr1wipA9iprdY
> .
@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:NP129499.RA88rz_2gl0WsS0Ot_Qachqgi7ZXnNZeTr1wipA9iprdY130_head
{
this:
np:hasAssertion
dgn-np:NP129499.RA88rz_2gl0WsS0Ot_Qachqgi7ZXnNZeTr1wipA9iprdY130_assertion
;
np:hasProvenance
dgn-np:NP129499.RA88rz_2gl0WsS0Ot_Qachqgi7ZXnNZeTr1wipA9iprdY130_provenance
;
np:hasPublicationInfo
dgn-np:NP129499.RA88rz_2gl0WsS0Ot_Qachqgi7ZXnNZeTr1wipA9iprdY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP129499.RA88rz_2gl0WsS0Ot_Qachqgi7ZXnNZeTr1wipA9iprdY130_assertion
a
np:Assertion
.
dgn-np:NP129499.RA88rz_2gl0WsS0Ot_Qachqgi7ZXnNZeTr1wipA9iprdY130_provenance
a
np:Provenance
.
dgn-np:NP129499.RA88rz_2gl0WsS0Ot_Qachqgi7ZXnNZeTr1wipA9iprdY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP129499.RA88rz_2gl0WsS0Ot_Qachqgi7ZXnNZeTr1wipA9iprdY130_assertion
{
miriam-gene:1544
a
ncit:C16612
.
lld:C0005695
a
ncit:C7057
.
dgn-gda:DGN8cbdf42e76f3753f95cbc54c0423f24e
sio:SIO_000628
miriam-gene:1544
,
lld:C0005695
;
a
sio:SIO_001121
.
}
dgn-np:NP129499.RA88rz_2gl0WsS0Ot_Qachqgi7ZXnNZeTr1wipA9iprdY130_provenance
{
dgn-np:NP129499.RA88rz_2gl0WsS0Ot_Qachqgi7ZXnNZeTr1wipA9iprdY130_assertion
dcterms:description
"[The results indicate that phenotypic differences in NAT2 alone or in combination with CYP1A2 might help explain the higher incidence rates of transitional cell bladder cancer in white cigarette smokers compared with black smokers.]. 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:18703023
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP129499.RA88rz_2gl0WsS0Ot_Qachqgi7ZXnNZeTr1wipA9iprdY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:07+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" .
}