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- NP316168.RAOhnhMnC0G8w7gPGLUwK8zr171vs5CxLX_XPyd_s3AL8130_assertion type Assertion NP316168.RAOhnhMnC0G8w7gPGLUwK8zr171vs5CxLX_XPyd_s3AL8130_head.
- NP316168.RAOhnhMnC0G8w7gPGLUwK8zr171vs5CxLX_XPyd_s3AL8130_assertion wasGeneratedBy ECO_0000203 NP316168.RAOhnhMnC0G8w7gPGLUwK8zr171vs5CxLX_XPyd_s3AL8130_provenance.
- NP316168.RAOhnhMnC0G8w7gPGLUwK8zr171vs5CxLX_XPyd_s3AL8130_assertion wasDerivedFrom befree-20150227 NP316168.RAOhnhMnC0G8w7gPGLUwK8zr171vs5CxLX_XPyd_s3AL8130_provenance.
- NP316168.RAOhnhMnC0G8w7gPGLUwK8zr171vs5CxLX_XPyd_s3AL8130_assertion SIO_000772 10428067 NP316168.RAOhnhMnC0G8w7gPGLUwK8zr171vs5CxLX_XPyd_s3AL8130_provenance.
- NP316168.RAOhnhMnC0G8w7gPGLUwK8zr171vs5CxLX_XPyd_s3AL8130_assertion evidence source_evidence_literature NP316168.RAOhnhMnC0G8w7gPGLUwK8zr171vs5CxLX_XPyd_s3AL8130_provenance.
- NP316168.RAOhnhMnC0G8w7gPGLUwK8zr171vs5CxLX_XPyd_s3AL8130_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." NP316168.RAOhnhMnC0G8w7gPGLUwK8zr171vs5CxLX_XPyd_s3AL8130_provenance.