Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_assertion> ?p ?o ?g. }
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- NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_assertion type Assertion NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_head.
- NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_assertion description "[In three patients, we detected genomic imbalances associated with the observed diaphragmatic hernia; a deletion of 8p22-p23.3, 14.2 Mb in size, a 340 kb duplication of Xq13.1 including the ephrin-B1 gene (EFNB1), and mosaicism for trisomy 2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_provenance.
- NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_assertion evidence source_evidence_literature NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_provenance.
- NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_assertion SIO_000772 21064195 NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_provenance.
- NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_assertion wasDerivedFrom befree-2016 NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_provenance.
- NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_assertion wasGeneratedBy ECO_0000203 NP851620.RAbQ5AtJxpAKl388gZ3R3JuYpuSvXq56FwHJy0M-vwLE4130_provenance.