@prefix orcid: .
@prefix this: .
@prefix rdfs: .
@prefix xsd: .
@prefix sio: .
@prefix ncit: .
@prefix lld: .
@prefix miriam-gene: .
@prefix miriam-pubmed: .
@prefix eco: .
@prefix wi: .
@prefix prov: .
@prefix pav: .
@prefix prv: .
@prefix dcterms: .
@prefix np: .
@prefix dgn-np: .
@prefix dgn-gda: .
@prefix dgn-void: .
dgn-np:NP253145.RAncVFz2A05ilihzbmnnQgU_gqx62mJWjkjU5nTTE769Q130_head {
this: np:hasAssertion dgn-np:NP253145.RAncVFz2A05ilihzbmnnQgU_gqx62mJWjkjU5nTTE769Q130_assertion;
np:hasProvenance dgn-np:NP253145.RAncVFz2A05ilihzbmnnQgU_gqx62mJWjkjU5nTTE769Q130_provenance;
np:hasPublicationInfo dgn-np:NP253145.RAncVFz2A05ilihzbmnnQgU_gqx62mJWjkjU5nTTE769Q130_publicationInfo;
a np:Nanopublication .
dgn-np:NP253145.RAncVFz2A05ilihzbmnnQgU_gqx62mJWjkjU5nTTE769Q130_assertion a np:Assertion .
dgn-np:NP253145.RAncVFz2A05ilihzbmnnQgU_gqx62mJWjkjU5nTTE769Q130_provenance a np:Provenance .
dgn-np:NP253145.RAncVFz2A05ilihzbmnnQgU_gqx62mJWjkjU5nTTE769Q130_publicationInfo a
np:PublicationInfo .
}
dgn-np:NP253145.RAncVFz2A05ilihzbmnnQgU_gqx62mJWjkjU5nTTE769Q130_assertion {
miriam-gene:412 a ncit:C16612 .
lld:C0333873 a ncit:C7057 .
dgn-gda:DGN3c25f0162a86275e38c9a9df0d0fb250 sio:SIO_000628 miriam-gene:412, lld:C0333873;
a sio:SIO_001121 .
}
dgn-np:NP253145.RAncVFz2A05ilihzbmnnQgU_gqx62mJWjkjU5nTTE769Q130_provenance {
dgn-np:NP253145.RAncVFz2A05ilihzbmnnQgU_gqx62mJWjkjU5nTTE769Q130_assertion dcterms:description
"[In cytopathologic examination, genomic amplification of TERC was found in 30 of 659 (4.6%) normal or benign cellular changes; in 23 of 170 (13.5%) atypical squamous cells of undetermined significance (ASCUS); in 8 of 28 (28.6%) atypical squamous cells with high-grade squamous intraepithelial lesion possible (ASC-H); and in 26 of 103 (25.2%) low-grade (LSIL) and 64 of 73 (87.7%) high-grade (HSIL) squamous intraepithelial lesions; with pairwise significant difference (P< 0.05) in each, except ASC-H and LSIL (chi(2) = 0.127, P = 0.72).]. 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:19389503;
prov:wasDerivedFrom dgn-void:befree-20150227;
prov:wasGeneratedBy eco:ECO_0000203 .
dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP253145.RAncVFz2A05ilihzbmnnQgU_gqx62mJWjkjU5nTTE769Q130_publicationInfo {
this: dcterms:created "2015-08-25T14:40:04+02:00"^^xsd:dateTime;
dcterms:rights ;
dcterms:rightsHolder dgn-void:IBIGroup;
dcterms:subject sio:SIO_000983;
prv:usedData dgn-void:disgenetv3.0rdf;
pav:authoredBy orcid:0000-0001-5999-6269, orcid:0000-0002-7534-7661, orcid:0000-0002-9383-528X,
orcid:0000-0003-0169-8159, orcid:0000-0003-1244-7654;
pav:createdBy orcid:0000-0003-0169-8159;
pav:version "v3.0.0.0" .
dgn-void:disgenetv3.0rdf pav:version "v3.0.0" .
}