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- NP213663.RAyycGy3x6s4rcJ3Zkf16zax40JU-nhBj6Gg53u4YOPc0130_assertion type Assertion NP213663.RAyycGy3x6s4rcJ3Zkf16zax40JU-nhBj6Gg53u4YOPc0130_head.
- NP213663.RAyycGy3x6s4rcJ3Zkf16zax40JU-nhBj6Gg53u4YOPc0130_assertion wasGeneratedBy ECO_0000203 NP213663.RAyycGy3x6s4rcJ3Zkf16zax40JU-nhBj6Gg53u4YOPc0130_provenance.
- NP213663.RAyycGy3x6s4rcJ3Zkf16zax40JU-nhBj6Gg53u4YOPc0130_assertion wasDerivedFrom lhgdn-20090331 NP213663.RAyycGy3x6s4rcJ3Zkf16zax40JU-nhBj6Gg53u4YOPc0130_provenance.
- NP213663.RAyycGy3x6s4rcJ3Zkf16zax40JU-nhBj6Gg53u4YOPc0130_assertion SIO_000772 15793844 NP213663.RAyycGy3x6s4rcJ3Zkf16zax40JU-nhBj6Gg53u4YOPc0130_provenance.
- NP213663.RAyycGy3x6s4rcJ3Zkf16zax40JU-nhBj6Gg53u4YOPc0130_assertion evidence source_evidence_literature NP213663.RAyycGy3x6s4rcJ3Zkf16zax40JU-nhBj6Gg53u4YOPc0130_provenance.
- NP213663.RAyycGy3x6s4rcJ3Zkf16zax40JU-nhBj6Gg53u4YOPc0130_assertion description "[We report a Chinese patient with amyloidotic polyneuropathy associated with a novel transthyretin mutation (V32A)...likely to be associated with late onset and low-penetrance phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP213663.RAyycGy3x6s4rcJ3Zkf16zax40JU-nhBj6Gg53u4YOPc0130_provenance.