@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk
> .
@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:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_head
{
this:
np:hasAssertion
dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_assertion
;
np:hasProvenance
dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_provenance
;
np:hasPublicationInfo
dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_assertion
a
np:Assertion
.
dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_provenance
a
np:Provenance
.
dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_assertion
{
miriam-gene:10
a
ncit:C16612
.
lld:C0302592
a
ncit:C7057
.
dgn-gda:DGN912de7dd7ea97320c3f90cd564d3f76b
sio:SIO_000628
miriam-gene:10
,
lld:C0302592
;
a
sio:SIO_001122
.
}
dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_provenance
{
dgn-np:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_assertion
dcterms:description
"[The results reported in this study suggest that NAT2 polymorphism is a genetic susceptibility factor involved in the carcinogenesis of cervical cancer, and also that the analysis of the allelic profile of populations in different geographic locations may help to understand the incidence of cervical cancer worldwide.]. 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:12474054
;
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:NP54067.RAiP6XkhCk4EGEsj-TkLnBiUq5VaTqv_BAN35sABCaMrk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:25+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" .
}