Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_assertion> ?p ?o ?g. }
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- NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_assertion type Assertion NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_head.
- NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_assertion wasGeneratedBy ECO_0000218 NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_provenance.
- NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_assertion wasDerivedFrom uniprot-2016 NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_provenance.
- NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_assertion SIO_000772 10494093 NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_provenance.
- NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_assertion evidence source_evidence_curated NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_provenance.
- NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_assertion description "[Identification and characterization of hydroxymethylbilane synthase mutations causing acute intermittent porphyria: evidence for an ancestral founder of the common G111R mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP397.RABwRB9A_PXw-AmDab5Lxok91URghwFfeYiJoqMp9Snu4130_provenance.