@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:NP781381.RA0zPgMHIvk3As6L6jGUty1jX5x8n2ja12t_xfJnadqAo130_head { this: np:hasAssertion dgn-np:NP781381.RA0zPgMHIvk3As6L6jGUty1jX5x8n2ja12t_xfJnadqAo130_assertion; np:hasProvenance dgn-np:NP781381.RA0zPgMHIvk3As6L6jGUty1jX5x8n2ja12t_xfJnadqAo130_provenance; np:hasPublicationInfo dgn-np:NP781381.RA0zPgMHIvk3As6L6jGUty1jX5x8n2ja12t_xfJnadqAo130_publicationInfo; a np:Nanopublication . dgn-np:NP781381.RA0zPgMHIvk3As6L6jGUty1jX5x8n2ja12t_xfJnadqAo130_assertion a np:Assertion . dgn-np:NP781381.RA0zPgMHIvk3As6L6jGUty1jX5x8n2ja12t_xfJnadqAo130_provenance a np:Provenance . dgn-np:NP781381.RA0zPgMHIvk3As6L6jGUty1jX5x8n2ja12t_xfJnadqAo130_publicationInfo a np:PublicationInfo . } dgn-np:NP781381.RA0zPgMHIvk3As6L6jGUty1jX5x8n2ja12t_xfJnadqAo130_assertion { miriam-gene:7012 a ncit:C16612 . lld:C0007137 a ncit:C7057 . dgn-gda:DGNfcfd42b0f8458f7d4c16501fe8c5c87e sio:SIO_000628 miriam-gene:7012, lld:C0007137; a sio:SIO_001121 . } dgn-np:NP781381.RA0zPgMHIvk3As6L6jGUty1jX5x8n2ja12t_xfJnadqAo130_provenance { dgn-np:NP781381.RA0zPgMHIvk3As6L6jGUty1jX5x8n2ja12t_xfJnadqAo130_assertion dcterms:description "[One hundred ten cervical specimens, which were collected from patients with various kinds of uterine cervix disease that was subsequently diagnosed as chronic cervicitis and with examination results negative for intraepithelial lesion or malignancy (NILM, n = 23), mild dysplasia (cervical intraepithelial neoplasia type 1 [CIN1], n = 37), moderate dysplasia (CIN2, n = 12), severe dysplasia (CIN3, n = 10), and squamous cell carcinoma (SCA, n = 28) confirmed by histologic diagnosis, were analyzed for the proportion of abnormal cells with TERC gain using a commercially available 2-color fluorescence in situ hybridization (FISH) probe.]. 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:20009881; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^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:NP781381.RA0zPgMHIvk3As6L6jGUty1jX5x8n2ja12t_xfJnadqAo130_publicationInfo { this: dcterms:created "2016-05-13T12:47:39+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }