Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_assertion> ?p ?o ?g. }
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- NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_assertion type Assertion NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_head.
- NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_assertion description "[Methemoglobinemia, the first hereditary disease to be identified that involved an enzyme deficiency, has been ascribed to mutations in the enzyme cytochrome b(5) reductase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_provenance.
- NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_assertion evidence source_evidence_literature NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_provenance.
- NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_assertion SIO_000772 14609324 NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_provenance.
- NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_assertion wasDerivedFrom befree-20150227 NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_provenance.
- NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_assertion wasGeneratedBy ECO_0000203 NP353751.RAGEfMc0GMMsj_rfDb9L1i_xb33TgsF0kGSmOKJwzd6jw130_provenance.