Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_assertion> ?p ?o ?g. }
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- NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_assertion type Assertion NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_head.
- NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_assertion wasGeneratedBy ECO_0000203 NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.
- NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_assertion wasDerivedFrom befree-20150227 NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.
- NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_assertion SIO_000772 20085575 NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.
- NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_assertion evidence source_evidence_literature NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.
- NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_assertion description "[The most frequent cytogenetic abnormalities were ETV6/RUNX1 fusion (16%) and trisomy 8 (14.6%).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP285284.RA-zgY_5UBW-sKC_7K95mfE7eo3duoXVNCA6GA2UrgHHA130_provenance.