Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_assertion> ?p ?o ?g. }
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- NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_assertion type Assertion NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_head.
- NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_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." NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_provenance.
- NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_assertion evidence source_evidence_literature NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_provenance.
- NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_assertion SIO_000772 19378506 NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_provenance.
- NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_assertion wasDerivedFrom befree-20140225 NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_provenance.
- NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_assertion wasGeneratedBy ECO_0000203 NP222055.RASDmjWAKV3nzDySGhysxJ_b_l3e3hKhGlUdIlVRtPQJg130_provenance.