Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_assertion> ?p ?o ?g. }
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- NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_assertion type Assertion NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_head.
- NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_assertion description "[Spinal muscular atrophy (SMA) is a common autosomal-recessive neuromuscular disorder caused by mutations in the survival motor neuron (SMN1) gene, affecting approximately 1 in 10,000 live births.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_provenance.
- NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_assertion evidence source_evidence_literature NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_provenance.
- NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_assertion SIO_000772 20494255 NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_provenance.
- NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_assertion wasDerivedFrom befree-2016 NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_provenance.
- NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_assertion wasGeneratedBy ECO_0000203 NP813991.RAAKFFRPOAscStPtVhfa2n-lYj40BCzseb3WoloPCJw_c130_provenance.