Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_assertion> ?p ?o ?g. }
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- NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_assertion type Assertion NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_head.
- NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_assertion description "[A novel missense mutation in codon 218 of the albumin gene in a distinct phenotype of familial dysalbuminemic hyperthyroxinemia in a Japanese kindred.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_provenance.
- NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_assertion evidence source_evidence_curated NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_provenance.
- NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_assertion SIO_000772 9329347 NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_provenance.
- NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_assertion wasDerivedFrom ctd_human-20130708 NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_provenance.
- NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_assertion wasGeneratedBy ECO_0000218 NP8317.RAAwWV4sS2O3YM29QDKXw0q2ZtU485Phd4XkVURyI9Jwk130_provenance.