Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_provenance.
- NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_assertion description "[We found only one mutation of the N-ras gene that was a 2-bp substitution of GGT(Gly) to GTC(Val) at codon 13 among 22 t(1;19)-ALL cases and five cell lines.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_provenance.
- NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_assertion evidence source_evidence_literature NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_provenance.
- NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_assertion SIO_000772 7727782 NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_provenance.
- NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_assertion wasDerivedFrom befree-20140225 NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_provenance.
- NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_assertion wasGeneratedBy ECO_0000203 NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP683839.RAU-D1A3Cz0_HlY77pBza5wRUOE96g4qpxHXAPyGDu8AQ130_provenance.