Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_assertion> ?p ?o ?g. }
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- NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_assertion type Assertion NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_head.
- NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_assertion description "[Allelic loss of 13q14 was observed in 63.2% patients, most of them showing D13S319 and D13S25 deletion; 11% of patients showed TP53 monosomy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_provenance.
- NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_assertion evidence source_evidence_literature NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_provenance.
- NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_assertion SIO_000772 14553950 NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_provenance.
- NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_assertion wasDerivedFrom befree-20150227 NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_provenance.
- NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_assertion wasGeneratedBy ECO_0000203 NP750762.RAU5meqRRxY_Bycu9xk9ikGHn8wtwgoDNVIa_dZqo-AMc130_provenance.