Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion type Assertion NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_head.
- NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion description "[Spinal muscular atrophy (SMA), the leading genetic cause of death in childhood, is an autosomal recessive neuromuscular disorder characterized by progressive muscle weakness, associated with deletions of the survival motor neuron (SMN) gene identified and mapped to chromosome 5q13.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
- NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion evidence source_evidence_literature NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
- NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion SIO_000772 19378506 NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
- NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion wasDerivedFrom befree-20140225 NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.
- NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_assertion wasGeneratedBy ECO_0000203 NP651020.RA_kIF-xVP3ditOiJX7hzV5D4j0CC9tyhP07Aov0XsuE4130_provenance.