Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_assertion> ?p ?o ?g. }
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- NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_assertion type Assertion NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_head.
- NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_assertion description "[We describe a 5-month-old boy with complex congenital heart defects (dTGA, DORV, VSD, ASD, and PDA), minor facial and ear anomalies, deep palmar creases, multiple vertebral anomalies, agenesis of the corpus callosum, and mosaic tetrasomy 8p (47,XY,+i(8)(p10)[88%]/46,XY[12%] in blood with normal chromosomes in cultured skin fibroblasts.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_provenance.
- NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_assertion evidence source_evidence_literature NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_provenance.
- NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_assertion SIO_000772 9415694 NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_provenance.
- NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_assertion wasDerivedFrom befree-20140225 NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_provenance.
- NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_assertion wasGeneratedBy ECO_0000203 NP786604.RAJpoPyWrLW42GWbfJeBf66U7amrBjNXtkfCMyisH_Ct4130_provenance.