Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_assertion> ?p ?o ?g. }
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- NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_assertion type Assertion NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_head.
- NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_assertion description "[Numerous non-synonymous mutations in FMO3 have been identified in patients suffering from this metabolic disorder (e.g., N61S, M66I, P153L, and R492W), but the molecular mechanism(s) underlying the functional deficit attributed to these alleles has not been elucidated.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_provenance.
- NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_assertion evidence source_evidence_literature NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_provenance.
- NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_assertion SIO_000772 17531949 NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_provenance.
- NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_assertion wasDerivedFrom befree-20150227 NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_provenance.
- NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_assertion wasGeneratedBy ECO_0000203 NP408589.RAhRhJXLEwkjZK-2mWYECOcVE6tSDT1czPJu1JTCwB4Vc130_provenance.