Matches in Nanopublications for { ?s ?p "[Niemann-Pick type C1 disease (NPC1) is an autosomal recessive neurovisceral storage disease caused by the mutation of NPC1 gene, resulting in perturbed intracellular transport of unesterified cholesterol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP391696.RAfFS7rrBDGryDLzM4ElhsdqI65Rp_L2AIClGVPpBI6Cs130_assertion description "[Niemann-Pick type C1 disease (NPC1) is an autosomal recessive neurovisceral storage disease caused by the mutation of NPC1 gene, resulting in perturbed intracellular transport of unesterified cholesterol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP391696.RAfFS7rrBDGryDLzM4ElhsdqI65Rp_L2AIClGVPpBI6Cs130_provenance.
- NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_assertion description "[Niemann-Pick type C1 disease (NPC1) is an autosomal recessive neurovisceral storage disease caused by the mutation of NPC1 gene, resulting in perturbed intracellular transport of unesterified cholesterol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP597232.RAbeJ-JpwLBBcMRqo7ofgISNfrSWPFjlY-KOnykWkaLt4130_provenance.
- assertion description "[Niemann-Pick type C1 disease (NPC1) is an autosomal recessive neurovisceral storage disease caused by the mutation of NPC1 gene, resulting in perturbed intracellular transport of unesterified cholesterol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP982227.RAvcXdNN352w9q3Xd-O9vG3_pQ3--oOXRfk7pOKdNHHUM130_assertion description "[Niemann-Pick type C1 disease (NPC1) is an autosomal recessive neurovisceral storage disease caused by the mutation of NPC1 gene, resulting in perturbed intracellular transport of unesterified cholesterol.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP982227.RAvcXdNN352w9q3Xd-O9vG3_pQ3--oOXRfk7pOKdNHHUM130_provenance.