Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_assertion> ?p ?o ?g. }
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- NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_assertion type Assertion NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_head.
- NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_assertion description "[The defect, however, is different from I-cell disease and pseudo-Hurler polydystrophy, two disorders of post-translational lysosomal enzyme biosynthesis, since complementation studies demonstrated recovery of intracellular beta-galactosidase and alpha-neuraminidase levels in heterokaryons.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_provenance.
- NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_assertion evidence source_evidence_literature NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_provenance.
- NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_assertion SIO_000772 7076257 NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_provenance.
- NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_assertion wasDerivedFrom befree-20140225 NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_provenance.
- NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_assertion wasGeneratedBy ECO_0000203 NP476086.RAX42TRRD11_5DcDPYCOaPsqgnFU08Gd9ur0IxCO6LHj4130_provenance.