@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP129753.RAefqTi0lXxBUrZlTqh46TqUF2LQhUAfddYoEOUJ57lAY
> .
@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/v3.0.0/void/
> .
dgn-np:NP129753.RAefqTi0lXxBUrZlTqh46TqUF2LQhUAfddYoEOUJ57lAY130_head
{
this:
np:hasAssertion
dgn-np:NP129753.RAefqTi0lXxBUrZlTqh46TqUF2LQhUAfddYoEOUJ57lAY130_assertion
;
np:hasProvenance
dgn-np:NP129753.RAefqTi0lXxBUrZlTqh46TqUF2LQhUAfddYoEOUJ57lAY130_provenance
;
np:hasPublicationInfo
dgn-np:NP129753.RAefqTi0lXxBUrZlTqh46TqUF2LQhUAfddYoEOUJ57lAY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP129753.RAefqTi0lXxBUrZlTqh46TqUF2LQhUAfddYoEOUJ57lAY130_assertion
a
np:Assertion
.
dgn-np:NP129753.RAefqTi0lXxBUrZlTqh46TqUF2LQhUAfddYoEOUJ57lAY130_provenance
a
np:Provenance
.
dgn-np:NP129753.RAefqTi0lXxBUrZlTqh46TqUF2LQhUAfddYoEOUJ57lAY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP129753.RAefqTi0lXxBUrZlTqh46TqUF2LQhUAfddYoEOUJ57lAY130_assertion
{
miriam-gene:10
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN80529a399c9566cc0afea5f623016eeb
sio:SIO_000628
miriam-gene:10
,
lld:C0027651
;
a
sio:SIO_001122
.
}
dgn-np:NP129753.RAefqTi0lXxBUrZlTqh46TqUF2LQhUAfddYoEOUJ57lAY130_provenance
{
dgn-np:NP129753.RAefqTi0lXxBUrZlTqh46TqUF2LQhUAfddYoEOUJ57lAY130_assertion
dcterms:description
"[Ethnic differences in the NAT2 genotype frequencies may be one of the important factors explaining variability in cancer incidence and drug toxicity. Our observations could be useful in assessing the susceptibility of different populations to cancer and c]. 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:20175805
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP129753.RAefqTi0lXxBUrZlTqh46TqUF2LQhUAfddYoEOUJ57lAY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:53+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}