Matches in Nanopublications for { ?s ?p "[Mutations in ATP8B1 cause familial intrahepatic cholestasis type 1, a spectrum of disorders characterized by intrahepatic cholestasis, reduced growth, deafness, and diarrhea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
Showing items 1 to 2 of
2
with 100 items per page.
- NP582906.RAGtdb4Mflno9UZ8nyhod0t8uGrncj8X3VKrA6wgmJkr0130_assertion description "[Mutations in ATP8B1 cause familial intrahepatic cholestasis type 1, a spectrum of disorders characterized by intrahepatic cholestasis, reduced growth, deafness, and diarrhea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP582906.RAGtdb4Mflno9UZ8nyhod0t8uGrncj8X3VKrA6wgmJkr0130_provenance.
- NP632980.RAIk4IMTe4-b7zNv5KVfUGIVCtLLT34VNWcVg919Z2gms130_assertion description "[Mutations in ATP8B1 cause familial intrahepatic cholestasis type 1, a spectrum of disorders characterized by intrahepatic cholestasis, reduced growth, deafness, and diarrhea.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632980.RAIk4IMTe4-b7zNv5KVfUGIVCtLLT34VNWcVg919Z2gms130_provenance.