Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_assertion> ?p ?o ?g. }
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- NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_assertion type Assertion NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_head.
- NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_assertion wasGeneratedBy ECO_0000203 NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_provenance.
- NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_assertion wasDerivedFrom befree-20150227 NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_provenance.
- NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_assertion SIO_000772 19100507 NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_provenance.
- NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_assertion evidence source_evidence_literature NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_provenance.
- NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_assertion description "[Trisomy 12 was seen in 12 (15.2%) cases, and was followed by 17p13.1 (TP53) deletions and 11q22.3 (ATM) deletions in 6 (7.6%) and 4 (5.1%) patients, respectively.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP753210.RABacUIlKDDLh0J9N2hpN_We25cBxBwuvecflClYcKoS8130_provenance.