Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_assertion type Assertion NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_head.
- 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.
- NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_assertion evidence source_evidence_literature NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_provenance.
- NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_assertion SIO_000772 18202104 NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_provenance.
- NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_assertion wasDerivedFrom befree-20140225 NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_provenance.
- NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_assertion wasGeneratedBy ECO_0000203 NP435337.RAEY7lCkmRX6qgN_VG0pucg4OYVuoRKBSVo-jEnu6ujd8130_provenance.