@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:NP1377681.RAw1P2wk1-0d8S_WtM4t8_cSCfNjJGU9Rv_tyLnMcvV9Y130_head { this: np:hasAssertion dgn-np:NP1377681.RAw1P2wk1-0d8S_WtM4t8_cSCfNjJGU9Rv_tyLnMcvV9Y130_assertion; np:hasProvenance dgn-np:NP1377681.RAw1P2wk1-0d8S_WtM4t8_cSCfNjJGU9Rv_tyLnMcvV9Y130_provenance; np:hasPublicationInfo dgn-np:NP1377681.RAw1P2wk1-0d8S_WtM4t8_cSCfNjJGU9Rv_tyLnMcvV9Y130_publicationInfo; a np:Nanopublication . dgn-np:NP1377681.RAw1P2wk1-0d8S_WtM4t8_cSCfNjJGU9Rv_tyLnMcvV9Y130_assertion a np:Assertion . dgn-np:NP1377681.RAw1P2wk1-0d8S_WtM4t8_cSCfNjJGU9Rv_tyLnMcvV9Y130_provenance a np:Provenance . dgn-np:NP1377681.RAw1P2wk1-0d8S_WtM4t8_cSCfNjJGU9Rv_tyLnMcvV9Y130_publicationInfo a np:PublicationInfo . } dgn-np:NP1377681.RAw1P2wk1-0d8S_WtM4t8_cSCfNjJGU9Rv_tyLnMcvV9Y130_assertion { miriam-gene:7157 a ncit:C16612 . lld:C0206708 a ncit:C7057 . dgn-gda:DGNe84f1bba2ecd5be9789c385dfc75163c sio:SIO_000628 miriam-gene:7157, lld:C0206708; a sio:SIO_001121 . } dgn-np:NP1377681.RAw1P2wk1-0d8S_WtM4t8_cSCfNjJGU9Rv_tyLnMcvV9Y130_provenance { dgn-np:NP1377681.RAw1P2wk1-0d8S_WtM4t8_cSCfNjJGU9Rv_tyLnMcvV9Y130_assertion dcterms:description "[To study the molecular abnormalities involved in the multistage development of cervical carcinoma (CC), we investigated the presence of oncogenic human papillomavirus (HPV) sequences, loss of heterozygosity (LOH), and microsatellite alterations at several genes/loci at 3p (3p14.2 at the FHIT gene, 3p14.3-21.1, 3p21, and 3p22-24.2), 9p21, RB and P53, and P53 gene point mutations in precisely microdissected archival tissues from 20 CCs and their accompanying precursor lesions (cervical intraepithelial neoplasia, CIN; n = 40) and normal epithelia (n = 20).]. 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:9242443; 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:NP1377681.RAw1P2wk1-0d8S_WtM4t8_cSCfNjJGU9Rv_tyLnMcvV9Y130_publicationInfo { this: dcterms:created "2016-05-13T12:52:10+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" . }