Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_assertion> ?p ?o ?g. }
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- NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_assertion type Assertion NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_head.
- NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_assertion description "[Because this region frequently is altered in neoplasms and in the genetic disease Beckwith-Wiedemann syndrome, we carried out a mutational analysis in tumor cell lines and Beckwith-Wiedemann syndrome samples that resulted in the identification of genetic alterations in the BWR1A gene: an insertion that introduced a stop codon in the breast cancer cell line BT549 and a point mutation in the rhabdomyosarcoma cell line TE125-T.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_provenance.
- NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_assertion evidence source_evidence_literature NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_provenance.
- NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_assertion SIO_000772 9520460 NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_provenance.
- NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_assertion wasDerivedFrom befree-2016 NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_provenance.
- NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_assertion wasGeneratedBy ECO_0000203 NP1391732.RAgik-4lgaV7LqRBt5oOZtvo85Ty3_1IQzu3kixvMSS_Q130_provenance.