Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_assertion> ?p ?o ?g. }
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- NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_assertion type Assertion NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_head.
- NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_assertion description "[Altogether eight abnormalities were repeatedly identified both as sole chromosomal anomalies and as part of more complex karyotypes: the structural rearrangements i(1)(q10), der(1:16)(q10;p10), del(1)(q11-12), del(3)(p12-13p14-21), and del(6)(q21-22) and the numerical aberrations +7, +18, and +20.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_provenance.
- NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_assertion evidence source_evidence_literature NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_provenance.
- NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_assertion SIO_000772 7536456 NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_provenance.
- NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_assertion wasDerivedFrom befree-20150227 NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_provenance.
- NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_assertion wasGeneratedBy ECO_0000203 NP942556.RAqgf4OpbJyTw4AlnPzejrPHQbtcANff8PJgDwk-diTuM130_provenance.