Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_assertion> ?p ?o ?g. }
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- NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_assertion type Assertion NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_head.
- NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_assertion description "[RSK4 is completely deleted in eight patients with the contiguous gene syndrome including MRX, partially deleted in a patient with DFN3 and present in patients with an Xq21 deletion and normal intellectual abilities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.
- NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_assertion evidence source_evidence_literature NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.
- NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_assertion SIO_000772 10644430 NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.
- NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_assertion wasDerivedFrom befree-20140225 NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.
- NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_assertion wasGeneratedBy ECO_0000203 NP561780.RAwGOCTAxia2nrfw0vZHI_gEosnHRwnizHb2wpBS6ZRUA130_provenance.