Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_assertion type Assertion NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_head.
- NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_assertion description "[Three siblings in their sixth and seventh decade with hexosaminidase A and B deficiency (adult form of GM2-gangliosidosis, variant O) developed early and severe sensory loss in addition to chronic motor neuron disease and cerebellar ataxia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_provenance.
- NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_assertion evidence source_evidence_literature NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_provenance.
- NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_assertion SIO_000772 8530938 NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_provenance.
- NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_assertion wasDerivedFrom befree-2016 NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_provenance.
- NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_assertion wasGeneratedBy ECO_0000203 NP1344482.RAsXWShdvmytOJ9e_FpNiv7KAJhLP_ufg-rc-r6iqRJvA130_provenance.