Matches in Nanopublications for { ?s ?p "[Type II recessive hereditary methaemoglobinaemia (RHM) is a rare disease due to generalized NADH-cytochrome b5 reductase (cytb5r) deficiency.]. 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.
- NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_assertion description "[Type II recessive hereditary methaemoglobinaemia (RHM) is a rare disease due to generalized NADH-cytochrome b5 reductase (cytb5r) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_provenance.
- NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_assertion description "[Type II recessive hereditary methaemoglobinaemia (RHM) is a rare disease due to generalized NADH-cytochrome b5 reductase (cytb5r) deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_provenance.