Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_assertion> ?p ?o ?g. }
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- NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_assertion type Assertion NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_head.
- NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_assertion description "[The majority of chromosomes displayed uniparental disomies, and microdeletions were present in genes with known importance for tumor formation (LRP1B, FHIT, and WWOX) or organogenesis (NEGR1 and ZFPM2), abnormalities not previously reported for pediatric WT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_provenance.
- NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_assertion evidence source_evidence_literature NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_provenance.
- NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_assertion SIO_000772 21947875 NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_provenance.
- NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_assertion wasDerivedFrom befree-20150227 NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_provenance.
- NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_assertion wasGeneratedBy ECO_0000203 NP982128.RAVhxQ_o5x0M7PbNq_Uk0ik5xl7Sa-uzEyqLUlp6mqs_U130_provenance.