@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP606874.RArk6n4KLwsM2oBo0XOYnnY9GFHbJdClOswMri3Ywy-94
> .
@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:NP606874.RArk6n4KLwsM2oBo0XOYnnY9GFHbJdClOswMri3Ywy-94130_head
{
this:
np:hasAssertion
dgn-np:NP606874.RArk6n4KLwsM2oBo0XOYnnY9GFHbJdClOswMri3Ywy-94130_assertion
;
np:hasProvenance
dgn-np:NP606874.RArk6n4KLwsM2oBo0XOYnnY9GFHbJdClOswMri3Ywy-94130_provenance
;
np:hasPublicationInfo
dgn-np:NP606874.RArk6n4KLwsM2oBo0XOYnnY9GFHbJdClOswMri3Ywy-94130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP606874.RArk6n4KLwsM2oBo0XOYnnY9GFHbJdClOswMri3Ywy-94130_assertion
a
np:Assertion
.
dgn-np:NP606874.RArk6n4KLwsM2oBo0XOYnnY9GFHbJdClOswMri3Ywy-94130_provenance
a
np:Provenance
.
dgn-np:NP606874.RArk6n4KLwsM2oBo0XOYnnY9GFHbJdClOswMri3Ywy-94130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP606874.RArk6n4KLwsM2oBo0XOYnnY9GFHbJdClOswMri3Ywy-94130_assertion
{
miriam-gene:29108
a
ncit:C16612
.
lld:C0206708
a
ncit:C7057
.
dgn-gda:DGN617d6090dcf297833db2071184198a22
sio:SIO_000628
miriam-gene:29108
,
lld:C0206708
;
a
sio:SIO_001121
.
}
dgn-np:NP606874.RArk6n4KLwsM2oBo0XOYnnY9GFHbJdClOswMri3Ywy-94130_provenance
{
dgn-np:NP606874.RArk6n4KLwsM2oBo0XOYnnY9GFHbJdClOswMri3Ywy-94130_assertion
dcterms:description
"[We have previously shown that human papillomavirus (HPV) genotyping, using the cobas HPV Test (Roche Molecular Systems, Pleasanton, CA), can be used to identify women with atypical squamous cells of undetermined significance (ASC-US) at the highest risk for cervical intraepithelial neoplasia (CIN) grade 2 or worse.]. 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:22261457
;
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:NP606874.RArk6n4KLwsM2oBo0XOYnnY9GFHbJdClOswMri3Ywy-94130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:04+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" .
}