Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_assertion> ?p ?o ?g. }
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- NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_assertion type Assertion NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_head.
- NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_assertion description "[Whole-exome sequencing identified HB as a genetically very simple tumour (2.9 mutations per tumour) with recurrent mutations in �-catenin (CTNNB1) (12/15 cases) and the transcription factor NFE2L2 (2/15 cases).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_provenance.
- NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_assertion evidence source_evidence_literature NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_provenance.
- NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_assertion SIO_000772 25135868 NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_provenance.
- NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_assertion wasDerivedFrom befree-2016 NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_provenance.
- NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_assertion wasGeneratedBy ECO_0000203 NP1211826.RAgzxQy4clSJgIgxo8IwzE0_3Pmd_JUr6JO6Uzng9_d1g130_provenance.