Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_assertion> ?p ?o ?g. }
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- NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_assertion type Assertion NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_head.
- NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_assertion description "[Inherited defects that reduce the concentration of BH4, therefore, in general, lead to phenylketonuria and to deficiencies of dopamine and serotonin, as tyrosine hydroxylase and tryptophan hydroxylase are the rate-limiting enzymes required for the synthesis of these neurotransmitters.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_provenance.
- NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_assertion evidence source_evidence_literature NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_provenance.
- NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_assertion SIO_000772 17513427 NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_provenance.
- NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_assertion wasDerivedFrom befree-20140225 NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_provenance.
- NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_assertion wasGeneratedBy ECO_0000203 NP870403.RAz8LcaKt7PtOkJcGJ8O1wAID21RKUNn5l_5KhHebrtvo130_provenance.