Matches in Nanopublications for { ?s ?p "[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."@en ?g. }
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- NP235403.RAjYZ-lyj7a3uc4AGIn3fHE0VCkjtLD3HQ78H9OZNwklA130_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." NP235403.RAjYZ-lyj7a3uc4AGIn3fHE0VCkjtLD3HQ78H9OZNwklA130_provenance.
- NP591528.RA4LEPr_6N_qxgewhK2OGeIGpdDsS-cHisH4N353r2_xo130_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." NP591528.RA4LEPr_6N_qxgewhK2OGeIGpdDsS-cHisH4N353r2_xo130_provenance.
- NP805444.RAJD-sFUl0lDtu7RVcxR-8rQ2VAUrteYB8J89ZWtwnAw4130_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." NP805444.RAJD-sFUl0lDtu7RVcxR-8rQ2VAUrteYB8J89ZWtwnAw4130_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.
- NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_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." NP585798.RAaqXA3EL9xNE8tRu65zNKZDfsimxj9hiHnSAPsPYEq2Q130_provenance.
- 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." provenance.
- 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." provenance.
- NP901454.RAKVuH---cvCqZ02C5s7vgGiZaSacH6gX4tWYZx4YiEYs130_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." NP901454.RAKVuH---cvCqZ02C5s7vgGiZaSacH6gX4tWYZx4YiEYs130_provenance.
- NP585799.RAhWS8pFSuunqBuQe31Mu2wFxVCHD6BCg3-q1XQLuWrck130_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." NP585799.RAhWS8pFSuunqBuQe31Mu2wFxVCHD6BCg3-q1XQLuWrck130_provenance.
- NP585800.RAq_DQdvGti2dtV0ovD4e3lf36AbLi4LYwaukaZfA5jFw130_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." NP585800.RAq_DQdvGti2dtV0ovD4e3lf36AbLi4LYwaukaZfA5jFw130_provenance.