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- NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_assertion type Assertion NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_head.
- NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_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." NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_provenance.
- NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_assertion evidence source_evidence_literature NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_provenance.
- NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_assertion SIO_000772 9329347 NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_provenance.
- NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_assertion wasDerivedFrom befree-20150227 NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_provenance.
- NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_assertion wasGeneratedBy ECO_0000203 NP233698.RAaHGB9Ov_g_Pxzn06jNx1JaAf10jUKFHNskvqpZVHcCQ130_provenance.