Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_assertion type Assertion NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_head.
- NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_assertion wasGeneratedBy ECO_0000203 NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_provenance.
- NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_assertion wasDerivedFrom befree-2016 NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_provenance.
- NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_assertion SIO_000772 21035104 NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_provenance.
- NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_assertion evidence source_evidence_literature NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_provenance.
- NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_assertion description "[PDYN mutations are identified in a small subset of ataxia families, indicating that SCA23 is an infrequent SCA type (∼0.5%) in the Netherlands and suggesting further genetic SCA heterogeneity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP849096.RAw41yQIdlDDzT_LzyDMsmglmFo1UFN7z8Uziejaucwh0130_provenance.