Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_assertion type Assertion NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_head.
- NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_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." NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_provenance.
- NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_assertion evidence source_evidence_literature NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_provenance.
- NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_assertion SIO_000772 19378506 NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_provenance.
- NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_assertion wasDerivedFrom befree-20150227 NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_provenance.
- NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_assertion wasGeneratedBy ECO_0000203 NP531785.RABwI3MW0LV2x7pI3ExM1w-9f3227FpGjaE7CEhSifaxo130_provenance.