Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_assertion type Assertion NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_head.
- NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_assertion description "[A genealogical and clinical study of the phenotypical variation within the Swedish transthyretin His88Arg (p. His108Arg) amyloidosis family.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_provenance.
- NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_assertion evidence source_evidence_literature NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_provenance.
- NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_assertion SIO_000772 25721874 NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_provenance.
- NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_assertion wasDerivedFrom befree-2016 NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_provenance.
- NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_assertion wasGeneratedBy ECO_0000203 NP1266642.RAKlJ_dl8QcXNcmsryTDJr3JV7fcMm0eQXd7Ml_x0oIcw130_provenance.