Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_assertion> ?p ?o ?g. }
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- NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_assertion type Assertion NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_head.
- NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_assertion description "[Transthyretin familial amyloid polyneuropathy is a rare, autosomal-dominant inherited multisystem disorder usually manifesting with a rapidly progressive, axonal, distally-symmetric polyneuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_provenance.
- NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_assertion evidence source_evidence_literature NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_provenance.
- NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_assertion SIO_000772 25526974 NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_provenance.
- NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_assertion wasDerivedFrom befree-2016 NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_provenance.
- NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_assertion wasGeneratedBy ECO_0000203 NP1249835.RA1xsSR36su8_pmCS3x5CIYGz5I2ZL2SQeR_2fx6g_XQs130_provenance.