Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_assertion> ?p ?o ?g. }
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- NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_assertion type Assertion NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_head.
- NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_assertion wasGeneratedBy ECO_0000203 NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_provenance.
- NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_assertion wasDerivedFrom befree-20150227 NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_provenance.
- NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_assertion SIO_000772 9627113 NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_provenance.
- NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_assertion evidence source_evidence_literature NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_provenance.
- NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_assertion description "[Investigation of mutations in exon 8, especially codon 273 mutation and mutant H2 alpha helix was considered to be a clinically useful approach for determining the prognosis of patients with NSCLC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762022.RAOmp_ps4BIuWOMtsnX8BlRa-6qT7hdCeOyIxDzSGw1DU130_provenance.