@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4
> .
@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:NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_head
{
this:
np:hasAssertion
dgn-np:NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_assertion
;
np:hasProvenance
dgn-np:NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_provenance
;
np:hasPublicationInfo
dgn-np:NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_assertion
a
np:Assertion
.
dgn-np:NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_provenance
a
np:Provenance
.
dgn-np:NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_assertion
{
miriam-gene:3251
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN4857ce843fe3cb731d4772c3cab59c61
sio:SIO_000628
miriam-gene:3251
,
lld:C0242379
;
a
sio:SIO_001122
.
}
dgn-np:NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_provenance
{
dgn-np:NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_assertion
dcterms:description
"[These findings suggest that the influence of NAT2 genotype on AL and MF and its interaction with GSTM1 genotype may be dose dependent. The NAT2 slow genotype, in particular when combined with the GSTM1 null genotype, may confer increased susceptibility to adduct formation, gene mutation, and lung cancer when the smoking dose is low.]. 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:11219770
;
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:NP57560.RAuP-Y8qhQ_QlnsTQgDrL5IdYAZ1eU4XAuNHCicRFIRT4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}