@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP308573.RAw8T7sB0S9K5pZ8Y3fDL246Pv5lGDNVpONq2TVD3scwY
> .
@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:NP308573.RAw8T7sB0S9K5pZ8Y3fDL246Pv5lGDNVpONq2TVD3scwY130_head
{
this:
np:hasAssertion
dgn-np:NP308573.RAw8T7sB0S9K5pZ8Y3fDL246Pv5lGDNVpONq2TVD3scwY130_assertion
;
np:hasProvenance
dgn-np:NP308573.RAw8T7sB0S9K5pZ8Y3fDL246Pv5lGDNVpONq2TVD3scwY130_provenance
;
np:hasPublicationInfo
dgn-np:NP308573.RAw8T7sB0S9K5pZ8Y3fDL246Pv5lGDNVpONq2TVD3scwY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP308573.RAw8T7sB0S9K5pZ8Y3fDL246Pv5lGDNVpONq2TVD3scwY130_assertion
a
np:Assertion
.
dgn-np:NP308573.RAw8T7sB0S9K5pZ8Y3fDL246Pv5lGDNVpONq2TVD3scwY130_provenance
a
np:Provenance
.
dgn-np:NP308573.RAw8T7sB0S9K5pZ8Y3fDL246Pv5lGDNVpONq2TVD3scwY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP308573.RAw8T7sB0S9K5pZ8Y3fDL246Pv5lGDNVpONq2TVD3scwY130_assertion
{
miriam-gene:81539
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGNc755c614cf5997b93f95bfaf9b9cda27
sio:SIO_000628
miriam-gene:81539
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP308573.RAw8T7sB0S9K5pZ8Y3fDL246Pv5lGDNVpONq2TVD3scwY130_provenance
{
dgn-np:NP308573.RAw8T7sB0S9K5pZ8Y3fDL246Pv5lGDNVpONq2TVD3scwY130_assertion
dcterms:description
"[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: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:NP308573.RAw8T7sB0S9K5pZ8Y3fDL246Pv5lGDNVpONq2TVD3scwY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:57+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" .
}