Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_assertion> ?p ?o ?g. }
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- NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_assertion type Assertion NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_head.
- NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_assertion wasGeneratedBy ECO_0000203 NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_provenance.
- NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_assertion wasDerivedFrom lhgdn-20090331 NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_provenance.
- NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_assertion SIO_000772 15793844 NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_provenance.
- NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_assertion evidence source_evidence_literature NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_provenance.
- NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_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." NP209976.RAgneiwTiI_1GCTzdfMjLSJrYLLJqpaTkZnaCJVb6ReBo130_provenance.