Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_assertion> ?p ?o ?g. }
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- NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_assertion type Assertion NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_head.
- NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_assertion description "[The aim of our study was to identify point mutations in a group of 606 patients diagnosed for spinal muscular atrophy with excluded biallelic loss of the SMN1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.
- NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_assertion evidence source_evidence_literature NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.
- NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_assertion SIO_000772 24844453 NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.
- NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_assertion wasDerivedFrom befree-2016 NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.
- NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_assertion wasGeneratedBy ECO_0000203 NP1184035.RATZJk6RO9jCZt2eICBzsSBD-x-IQxUAlVh0NttPOKNzw130_provenance.