Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_assertion> ?p ?o ?g. }
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- NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_assertion type Assertion NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_head.
- NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_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." NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_provenance.
- NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_assertion evidence source_evidence_literature NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_provenance.
- NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_assertion SIO_000772 7727782 NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_provenance.
- NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_assertion wasDerivedFrom befree-20140225 NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_provenance.
- NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_assertion wasGeneratedBy ECO_0000203 NP312015.RAEcg0H6GDX_nTV-_Ra9m9ZOJxEkKsL3fdjptgHcoqI48130_provenance.