Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_assertion> ?p ?o ?g. }
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- NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_assertion type Assertion NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_head.
- NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_assertion description "[Molybdenum cofactor deficiency and isolated sulfite oxidase deficiency are autosomal recessive inborn errors of metabolism with severe neurological symptoms resulting from a lack of sulfite oxidase activity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_provenance.
- NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_assertion evidence source_evidence_literature NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_provenance.
- NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_assertion SIO_000772 12533804 NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_provenance.
- NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_assertion wasDerivedFrom befree-2016 NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_provenance.
- NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_assertion wasGeneratedBy ECO_0000203 NP380670.RAA9fL7h8LEbpSiMa1mMNuAup4P__MO5h1W1eIUkw2l9c130_provenance.