Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_assertion> ?p ?o ?g. }
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- NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_assertion type Assertion NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_head.
- NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_assertion description "[Among 34 tissues specimens surgically resected from 30 patients and 5 cell lines of human HCC, only two had ras point mutations; in one case, codon 12 of c-Ki-ras was altered from GGT, coding glycine, to GTT, coding valine; in the other case, codon 61 of N-ras was altered from CAA, coding glutamine, to AAA, coding lysine.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_provenance.
- NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_assertion evidence source_evidence_literature NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_provenance.
- NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_assertion SIO_000772 2542205 NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_provenance.
- NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_assertion wasDerivedFrom befree-20140225 NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_provenance.
- NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_assertion wasGeneratedBy ECO_0000203 NP279804.RAofw9jGFRqFKL0K6yrqLm-xcDtPrubY952Vt4MywOkns130_provenance.