Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_assertion> ?p ?o ?g. }
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- NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_assertion type Assertion NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_head.
- NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_assertion description "[We found missense mutations of AAC (Asn) to AGC (Ser) at DCC codon 176 in one cell line and ACC (Thr) to ATC (Ile) at codon 1105 in one cell line and tumor, respectively; polymorphisms of CGA (Arg) to GGA (Gly) at codon 201 and TTT (Phe) to TTG (Leu) at codon 951 in most of the cell lines and tumors; and a silent mutation of GAG (Glu) to GAA (Glu) at codon 118 in four cell lines and five primary tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_provenance.
- NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_assertion evidence source_evidence_literature NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_provenance.
- NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_assertion SIO_000772 9288786 NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_provenance.
- NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_assertion wasDerivedFrom befree-2016 NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_provenance.
- NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_assertion wasGeneratedBy ECO_0000203 NP1380114.RAAggPFmC6wZpzGRf7AW1ETgv75paA2AOCdtS_npfbExg130_provenance.