Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_assertion> ?p ?o ?g. }
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- NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_assertion type Assertion NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_head.
- NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_assertion description "[We report a familial recombination of a pericentric inversion of chromosome 10 resulting in 2 affected relatives who had 10p trisomy and 10q monosomy with the karyotypic abnormality designated rec(10) dup p,inv(10) (p11.2q26).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_provenance.
- NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_assertion evidence source_evidence_literature NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_provenance.
- NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_assertion SIO_000772 8209887 NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_provenance.
- NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_assertion wasDerivedFrom befree-20140225 NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_provenance.
- NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_assertion wasGeneratedBy ECO_0000203 NP662432.RArSjEtkAv84jslHtEz4iydm9gC-8enF8zOwAbxDvXuPI130_provenance.