Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_assertion> ?p ?o ?g. }
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- NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_assertion type Assertion NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_head.
- NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_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." NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_provenance.
- NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_assertion evidence source_evidence_literature NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_provenance.
- NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_assertion SIO_000772 17513427 NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_provenance.
- NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_assertion wasDerivedFrom befree-2016 NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_provenance.
- NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_assertion wasGeneratedBy ECO_0000203 NP610860.RA6lfVgRL-3GJZaN6M-naBOPB7FA-Ry4_EyYOkG0TcL1k130_provenance.