Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_assertion> ?p ?o ?g. }
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- NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_assertion type Assertion NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_head.
- NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_assertion description "[We assessed a family in which the translocation between chromosomes 12 and 16 segregates; one of the eight progenies with the karyotype 47,XY,+21,t(12;16)(q24;q24) was heterozygote for the translocation and presented with Down syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.
- NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_assertion evidence source_evidence_literature NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.
- NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_assertion SIO_000772 18990986 NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.
- NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_assertion wasDerivedFrom befree-20140225 NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.
- NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_assertion wasGeneratedBy ECO_0000203 NP661076.RAYTdwpxoLSUgo_7bPD78rdvYnWZ5TuncFMKIy56Krruo130_provenance.