@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP309111.RAEwo1vCHqWX9EPte4nPwVT0LTBWzFOP326RfGQ4Lvmw4
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP309111.RAEwo1vCHqWX9EPte4nPwVT0LTBWzFOP326RfGQ4Lvmw4130_head
{
this:
np:hasAssertion
dgn-np:NP309111.RAEwo1vCHqWX9EPte4nPwVT0LTBWzFOP326RfGQ4Lvmw4130_assertion
;
np:hasProvenance
dgn-np:NP309111.RAEwo1vCHqWX9EPte4nPwVT0LTBWzFOP326RfGQ4Lvmw4130_provenance
;
np:hasPublicationInfo
dgn-np:NP309111.RAEwo1vCHqWX9EPte4nPwVT0LTBWzFOP326RfGQ4Lvmw4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP309111.RAEwo1vCHqWX9EPte4nPwVT0LTBWzFOP326RfGQ4Lvmw4130_assertion
a
np:Assertion
.
dgn-np:NP309111.RAEwo1vCHqWX9EPte4nPwVT0LTBWzFOP326RfGQ4Lvmw4130_provenance
a
np:Provenance
.
dgn-np:NP309111.RAEwo1vCHqWX9EPte4nPwVT0LTBWzFOP326RfGQ4Lvmw4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP309111.RAEwo1vCHqWX9EPte4nPwVT0LTBWzFOP326RfGQ4Lvmw4130_assertion
{
miriam-gene:10
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGN381ccdd541659b2c840b574b84bb9984
sio:SIO_000628
miriam-gene:10
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP309111.RAEwo1vCHqWX9EPte4nPwVT0LTBWzFOP326RfGQ4Lvmw4130_provenance
{
dgn-np:NP309111.RAEwo1vCHqWX9EPte4nPwVT0LTBWzFOP326RfGQ4Lvmw4130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP309111.RAEwo1vCHqWX9EPte4nPwVT0LTBWzFOP326RfGQ4Lvmw4130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:05+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}