Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_assertion> ?p ?o ?g. }
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- NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_assertion type Assertion NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_head.
- NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_assertion description "[Mutations in the BSCL2 gene have recently been identified in families with (SPG17-linked) Silver syndrome-type hereditary spastic paraparesis as well as in families with distal hereditary motor neuropathy (HMN).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_provenance.
- NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_assertion evidence source_evidence_literature NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_provenance.
- NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_assertion SIO_000772 16427281 NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_provenance.
- NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_assertion wasDerivedFrom befree-20150227 NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_provenance.
- NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_assertion wasGeneratedBy ECO_0000203 NP883897.RASc3davuoFricfsD1_Xhtq6t6Os98xjSjGSjyGzbVNsI130_provenance.