Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_assertion> ?p ?o ?g. }
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- NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_assertion type Assertion NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_head.
- NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_assertion description "[Spinal muscular atrophy with respiratory distress type 1 (SMARD1) is a rare autosomal recessive neuromuscular disease of unknown prevalence characterized by degeneration of anterior horn alpha-motoneurons and manifesting in the first 6months of life as life-threatening irreversible diaphragmatic paralysis associated with progressive symmetrical muscular weakness (distal lower limbs mainly involved), muscle atrophy, and peripheral sensory neuropathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_provenance.
- NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_assertion evidence source_evidence_literature NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_provenance.
- NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_assertion SIO_000772 16964485 NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_provenance.
- NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_assertion wasDerivedFrom befree-20140225 NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_provenance.
- NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_assertion wasGeneratedBy ECO_0000203 NP705435.RAsAIGCKPxb3gEBvD1Ac87v1zVvyDN4uap9NekkviJd8Q130_provenance.