Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_assertion> ?p ?o ?g. }
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- NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_assertion type Assertion NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_head.
- NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_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." NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_provenance.
- NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_assertion evidence source_evidence_literature NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_provenance.
- NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_assertion SIO_000772 21947875 NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_provenance.
- NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_assertion wasDerivedFrom befree-20140225 NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_provenance.
- NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_assertion wasGeneratedBy ECO_0000203 NP684424.RAzXXfJrP4RYsuHrYHlCV8gKvvSgfi5Z5RmA60gCOgw1k130_provenance.