Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_assertion> ?p ?o ?g. }
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- NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_assertion type Assertion NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_head.
- NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_assertion wasGeneratedBy ECO_0000203 NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_provenance.
- NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_assertion wasDerivedFrom befree-20150227 NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_provenance.
- NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_assertion SIO_000772 10428067 NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_provenance.
- NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_assertion evidence source_evidence_literature NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_provenance.
- NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_assertion description "[A survey of fibroblasts and lymphoblasts demonstrated that lack of activity was associated with LINCL arising from mutations in the CLN2 gene but not other neuronal ceroid lipofuscinoses (NCLs), including the CLN6 variant LINCL, classical infantile NCL, classical juvenile NCL, and adult NCL (Kufs' disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP915707.RAt7g1QSlTrX2Vmi4on4caOKqTxaGUpgvvC1-0d0mLsK4130_provenance.