Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_assertion> ?p ?o ?g. }
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- NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_assertion type Assertion NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_head.
- NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_assertion description "[From our results we extend the SPG11 associated phenotype to comprise also Kjellin syndrome, previously found to be associated with mutations in the SPG15 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_provenance.
- NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_assertion evidence source_evidence_literature NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_provenance.
- NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_assertion SIO_000772 19194956 NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_provenance.
- NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_assertion wasDerivedFrom befree-2016 NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_provenance.
- NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_assertion wasGeneratedBy ECO_0000203 NP718796.RASmWYph60FHL0T46VfcPERfTAKX26t4U_c8kAhlHqctE130_provenance.