Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_assertion type Assertion NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_head.
- NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_assertion wasGeneratedBy ECO_0000203 NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_provenance.
- NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_assertion wasDerivedFrom gad-20150221 NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_provenance.
- NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_assertion SIO_000772 17594340 NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_provenance.
- NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_assertion evidence source_evidence_literature NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_provenance.
- NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_assertion description "[Seven novel mutations and four exon deletions in a collection of Norwegian patients with SPG4 hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP63511.RAnfzEFXoGfMbvkhlYLHq_wdCLI6aWVS8NPp-uLCJg01M130_provenance.