Matches in Nanopublications for { ?s ?p "[It is commonly caused by defects in the peroxisome transporter, PEX7 (RCDP1), and less frequently due to defects in the peroxisomal enzymes required to initiate plasmalogen synthesis, GNPAT (RCDP2) and AGPS (RCDP3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP244.RA6VbhbSHOAYFuVuhcPtHFL6am8zxEoeZXzP_hNupnvd0130_assertion description "[It is commonly caused by defects in the peroxisome transporter, PEX7 (RCDP1), and less frequently due to defects in the peroxisomal enzymes required to initiate plasmalogen synthesis, GNPAT (RCDP2) and AGPS (RCDP3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP244.RA6VbhbSHOAYFuVuhcPtHFL6am8zxEoeZXzP_hNupnvd0130_provenance.
- NP20.RAX_yxGjUgEs4jtzEfN4Oe_OdIvJlb7disynXUO5TYnO0130_assertion description "[It is commonly caused by defects in the peroxisome transporter, PEX7 (RCDP1), and less frequently due to defects in the peroxisomal enzymes required to initiate plasmalogen synthesis, GNPAT (RCDP2) and AGPS (RCDP3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP20.RAX_yxGjUgEs4jtzEfN4Oe_OdIvJlb7disynXUO5TYnO0130_provenance.
- NP6805.RAMnet_VmgPm9K5Ghvfad6pmdQoDzSMovJMXwjvIZVqhY130_assertion description "[It is commonly caused by defects in the peroxisome transporter, PEX7 (RCDP1), and less frequently due to defects in the peroxisomal enzymes required to initiate plasmalogen synthesis, GNPAT (RCDP2) and AGPS (RCDP3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6805.RAMnet_VmgPm9K5Ghvfad6pmdQoDzSMovJMXwjvIZVqhY130_provenance.