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- source_evidence_literature type ECO_0000212 NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_provenance.
- NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_assertion description "[We identified RAS mutations in 16 out of 57 (28.1%) FAs, 2 out of 8 (25%) NWDTCs, 8 out of 42 (19.0%) FVPTCs, 2 out of 10 (20.0%) FTCs, 1 out of 12 (8.3%) Hurthle cell variants of FA, 3 out of 46 (6.5%) goiters, 1 out of 18 (5.6%) hyperplastic nodules, 3 out of 56 (5.4%) micro PTCs, 2 out of 115 (1.7%) PTCs, 0 out of 7 (0%) Hurthle cell variants of FTC, and 0 out of 10 (0%) HT lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_provenance.
- NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_assertion evidence source_evidence_literature NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_provenance.
- NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_assertion SIO_000772 24222113 NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_provenance.
- NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_assertion wasDerivedFrom befree-20150227 NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_provenance.
- NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_assertion wasGeneratedBy ECO_0000203 NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP788478.RAW_37qEzx9I5y00L0SiZfpGMkj_bRRCMUujAh5SiE19o130_provenance.