Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_assertion> ?p ?o ?g. }
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- NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_assertion type Assertion NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_head.
- NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_assertion wasGeneratedBy ECO_0000218 NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_provenance.
- NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_assertion wasDerivedFrom uniprot-20150221 NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_provenance.
- NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_assertion SIO_000772 1400360 NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_provenance.
- NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_assertion evidence source_evidence_curated NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_provenance.
- NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_assertion description "[Enzymatic instability of NADH-cytochrome b5 reductase as a cause of hereditary methemoglobinemia type I (red cell type).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP632.RAcfqxO9dwwZZHaRt_g0HS422Ql_ZvFwLMGVa15Cme-ww130_provenance.