Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_assertion> ?p ?o ?g. }
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- NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_assertion type Assertion NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_head.
- NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_assertion description "[By array comparative genomic hybridization (array-CGH), we identified a small duplication at Xq28 in a large family with a severe form of MR associated with progressive spasticity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.
- NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_assertion evidence source_evidence_literature NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.
- NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_assertion SIO_000772 16080119 NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.
- NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_assertion wasDerivedFrom befree-20140225 NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.
- NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_assertion wasGeneratedBy ECO_0000203 NP179624.RAsJFkkmls4ehiw12hEgZ79j5w7txn99_xplWORM8Dm1Q130_provenance.