Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_assertion> ?p ?o ?g. }
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- NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_assertion type Assertion NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_head.
- NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_assertion description "[Further analyses after birth, using C-banding, NOR staining and fluorescence in situ hybridization (FISH) with telomeric probes, revealed that it was the result of an unbalanced de novo t(11;14)(p15;p13) translocation leading to partial 11p trisomy and to BWS.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_provenance.
- NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_assertion evidence source_evidence_literature NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_provenance.
- NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_assertion SIO_000772 11241533 NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_provenance.
- NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_assertion wasDerivedFrom befree-20140225 NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_provenance.
- NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_assertion wasGeneratedBy ECO_0000203 NP684130.RA54JZ3nYB-QTg1sMlLbz1x-kEBPEruLvjtvKMdCuT6RY130_provenance.