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- source_evidence_literature type ECO_0000212 NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_provenance.
- NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_assertion 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." NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_provenance.
- NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_assertion evidence source_evidence_literature NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_provenance.
- NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_assertion SIO_000772 19389503 NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_provenance.
- NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_assertion wasDerivedFrom befree-2016 NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_provenance.
- NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_assertion wasGeneratedBy ECO_0000203 NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_provenance.
- befree-2016 importedOn "2016-02-19" NP734331.RAI6vvAIDKq0pBn6xWGZ3QCYJmd-N4NsD6rWq_8bEg55g130_provenance.