Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_assertion> ?p ?o ?g. }
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- NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_assertion type Assertion NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_head.
- NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_assertion description "[Restudy of the original DFN-1 family showed that the deafness is part of a progressive X linked recessive syndrome, which includes visual disability leading to cortical blindness, dystonia, fractures, and mental deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_provenance.
- NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_assertion evidence source_evidence_literature NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_provenance.
- NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_assertion SIO_000772 7643352 NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_provenance.
- NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_assertion wasDerivedFrom befree-20140225 NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_provenance.
- NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_assertion wasGeneratedBy ECO_0000203 NP484343.RAlmtPNSXxhsKYdgF1HmgbiXrKz6C5LK4cv3ygKk-H1yA130_provenance.