Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_assertion> ?p ?o ?g. }
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- NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_assertion type Assertion NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_head.
- NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_assertion description "[These two sphingolipidoses are characterized by a heritable absence of beta-hexosaminidase A resulting in defective GM2 ganglioside degradation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_provenance.
- NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_assertion evidence source_evidence_literature NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_provenance.
- NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_assertion SIO_000772 7550345 NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_provenance.
- NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_assertion wasDerivedFrom befree-2016 NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_provenance.
- NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_assertion wasGeneratedBy ECO_0000203 NP1312182.RAcQ9Xhid69WzW2viTIQCM0tw77G_wImzafTj8Oy2_Cfg130_provenance.