Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_provenance.
- NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_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." NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_provenance.
- NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_assertion evidence source_evidence_literature NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_provenance.
- NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_assertion SIO_000772 24222113 NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_provenance.
- NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_assertion wasDerivedFrom befree-20150227 NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_provenance.
- NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_assertion wasGeneratedBy ECO_0000203 NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP670654.RAAt_yukEL0hKqkwxvS5yzlA-Jbnv5uTbzV-x8jDMO88w130_provenance.