Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_assertion> ?p ?o ?g. }
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- NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_assertion type Assertion NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_head.
- NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_assertion description "[Patients were classified according to age of onset, clinical pattern, and associated neurological signs into `ULD-like` and `not ULD-like.` After exclusion of mutations in cystatin B (CSTB), DNA was examined for sequence variation in SCARB2 and PRICKLE1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_provenance.
- NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_assertion evidence source_evidence_literature NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_provenance.
- NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_assertion SIO_000772 19847901 NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_provenance.
- NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_assertion wasDerivedFrom befree-20140225 NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_provenance.
- NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_assertion wasGeneratedBy ECO_0000203 NP317638.RA6LVexS6MFKBDRte5O9EuijmwrDHsKXh87aQ0ZuY71O0130_provenance.