Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_assertion> ?p ?o ?g. }
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- NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_assertion type Assertion NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_head.
- NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_assertion wasGeneratedBy ECO_0000203 NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_provenance.
- NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_assertion wasDerivedFrom befree-20150227 NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_provenance.
- NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_assertion SIO_000772 17187067 NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_provenance.
- NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_assertion evidence source_evidence_literature NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_provenance.
- NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_assertion description "[NLSDM is distinct from Chanarin-Dorfman syndrome, which is characterized by neutral lipid storage disease with ichthyosis, mild myopathy and hepatomegaly due to mutations in ABHD5 (also known as CGI-58).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP901439.RAbTCH5jfoAkvk4QEZe6l2sjvFWGDSzZykBdmPfp0SnR4130_provenance.