@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP412216.RAcd30NfAxYZW6x1zJI_bLdNIxF7ecQ3nLB5x2GsmGXsE
> .
@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:NP412216.RAcd30NfAxYZW6x1zJI_bLdNIxF7ecQ3nLB5x2GsmGXsE130_head
{
this:
np:hasAssertion
dgn-np:NP412216.RAcd30NfAxYZW6x1zJI_bLdNIxF7ecQ3nLB5x2GsmGXsE130_assertion
;
np:hasProvenance
dgn-np:NP412216.RAcd30NfAxYZW6x1zJI_bLdNIxF7ecQ3nLB5x2GsmGXsE130_provenance
;
np:hasPublicationInfo
dgn-np:NP412216.RAcd30NfAxYZW6x1zJI_bLdNIxF7ecQ3nLB5x2GsmGXsE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP412216.RAcd30NfAxYZW6x1zJI_bLdNIxF7ecQ3nLB5x2GsmGXsE130_assertion
a
np:Assertion
.
dgn-np:NP412216.RAcd30NfAxYZW6x1zJI_bLdNIxF7ecQ3nLB5x2GsmGXsE130_provenance
a
np:Provenance
.
dgn-np:NP412216.RAcd30NfAxYZW6x1zJI_bLdNIxF7ecQ3nLB5x2GsmGXsE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP412216.RAcd30NfAxYZW6x1zJI_bLdNIxF7ecQ3nLB5x2GsmGXsE130_assertion
{
miriam-gene:1154
a
ncit:C16612
.
lld:C0333875
a
ncit:C7057
.
dgn-gda:DGN2562275baf3a2dba9c24a2afb2e1a329
sio:SIO_000628
miriam-gene:1154
,
lld:C0333875
;
a
sio:SIO_001121
.
}
dgn-np:NP412216.RAcd30NfAxYZW6x1zJI_bLdNIxF7ecQ3nLB5x2GsmGXsE130_provenance
{
dgn-np:NP412216.RAcd30NfAxYZW6x1zJI_bLdNIxF7ecQ3nLB5x2GsmGXsE130_assertion
dcterms:description
"[If manual cytology were to be used to refer all cases of HSIL and cancer to colposcopy and biopsy, 23 lesions that had to be removed would have been discovered (2 CIN2, 11 CIN3/CIS, and 10 cancers), for a sensitivity of 25.0+/-5.2% at specificity of 99.9+/-0.1%.]. 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:15750205
;
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:NP412216.RAcd30NfAxYZW6x1zJI_bLdNIxF7ecQ3nLB5x2GsmGXsE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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: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" .
}