Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_assertion type Assertion NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_head.
- NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_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." NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_provenance.
- NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_assertion evidence source_evidence_literature NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_provenance.
- NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_assertion SIO_000772 19847901 NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_provenance.
- NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_assertion wasDerivedFrom befree-2016 NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_provenance.
- NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_assertion wasGeneratedBy ECO_0000203 NP771013.RACA1GGgKNhtMupx7O0YiBHh2kMxxPDQgJZo3dzIwH6tY130_provenance.