Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_assertion type Assertion NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_head.
- NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_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." NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_provenance.
- NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_assertion evidence source_evidence_literature NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_provenance.
- NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_assertion SIO_000772 7536456 NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_provenance.
- NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_assertion wasDerivedFrom befree-2016 NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_provenance.
- NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_assertion wasGeneratedBy ECO_0000203 NP1311291.RAYsONrrNtf3PoPghvD9jA55hHXA0igvd0usJBWKHk8D4130_provenance.