Matches in Nanopublications for { ?s ?p "[FIC1-defective progressive familial intrahepatic cholestasis (previously Byler disease) is determined by mutations in the FIC1 gene, coding for P-type ATPases of unknown physiological function, while a second form (bile salt export pump defective progressive familial intrahepatic cholestatis) is caused by a defective function of the canalicular bile salt export pump.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP298012.RAthL6fXSeN92YUD0ZozuAPArFY2ZqmDwEBjzILg2bNQs130_assertion description "[FIC1-defective progressive familial intrahepatic cholestasis (previously Byler disease) is determined by mutations in the FIC1 gene, coding for P-type ATPases of unknown physiological function, while a second form (bile salt export pump defective progressive familial intrahepatic cholestatis) is caused by a defective function of the canalicular bile salt export pump.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP298012.RAthL6fXSeN92YUD0ZozuAPArFY2ZqmDwEBjzILg2bNQs130_provenance.
- NP209356.RANZrSrDXZeZ_CXNLeBLg8KLeUWC7gm7TkMYgzvJ4gA6w130_assertion description "[FIC1-defective progressive familial intrahepatic cholestasis (previously Byler disease) is determined by mutations in the FIC1 gene, coding for P-type ATPases of unknown physiological function, while a second form (bile salt export pump defective progressive familial intrahepatic cholestatis) is caused by a defective function of the canalicular bile salt export pump.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP209356.RANZrSrDXZeZ_CXNLeBLg8KLeUWC7gm7TkMYgzvJ4gA6w130_provenance.