Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_assertion> ?p ?o ?g. }
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- NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_assertion type Assertion NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_head.
- 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.
- NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_assertion evidence source_evidence_literature NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_provenance.
- NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_assertion SIO_000772 18202104 NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_provenance.
- NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_assertion wasDerivedFrom befree-20140225 NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_provenance.
- NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_assertion wasGeneratedBy ECO_0000203 NP865088.RA4UKymW7-OF_so8CS5_mm7aJzJFEMTm76lwOt-FRWxDM130_provenance.