Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_assertion> ?p ?o ?g. }
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- NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_assertion type Assertion NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_head.
- NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_assertion wasGeneratedBy ECO_0000203 NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.
- NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_assertion wasDerivedFrom befree-20150227 NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.
- NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_assertion SIO_000772 18853458 NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.
- NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_assertion evidence source_evidence_literature NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.
- NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_assertion description "[Complicated forms of autosomal dominant hereditary spastic paraplegia are frequent in SPG10.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP524199.RA0WWxH22cOI6G5_mcIpflMTgXwA4ePLezLhumOzVepSw130_provenance.