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- NP965243.RAkVYL-xnZtV7-xeykch6ZJjBGx8Ubf4XwT6KQXkfUHME130_assertion type Assertion NP965243.RAkVYL-xnZtV7-xeykch6ZJjBGx8Ubf4XwT6KQXkfUHME130_head.
- NP965243.RAkVYL-xnZtV7-xeykch6ZJjBGx8Ubf4XwT6KQXkfUHME130_assertion wasGeneratedBy ECO_0000203 NP965243.RAkVYL-xnZtV7-xeykch6ZJjBGx8Ubf4XwT6KQXkfUHME130_provenance.
- NP965243.RAkVYL-xnZtV7-xeykch6ZJjBGx8Ubf4XwT6KQXkfUHME130_assertion wasDerivedFrom befree-2016 NP965243.RAkVYL-xnZtV7-xeykch6ZJjBGx8Ubf4XwT6KQXkfUHME130_provenance.
- NP965243.RAkVYL-xnZtV7-xeykch6ZJjBGx8Ubf4XwT6KQXkfUHME130_assertion SIO_000772 22387303 NP965243.RAkVYL-xnZtV7-xeykch6ZJjBGx8Ubf4XwT6KQXkfUHME130_provenance.
- NP965243.RAkVYL-xnZtV7-xeykch6ZJjBGx8Ubf4XwT6KQXkfUHME130_assertion evidence source_evidence_literature NP965243.RAkVYL-xnZtV7-xeykch6ZJjBGx8Ubf4XwT6KQXkfUHME130_provenance.
- NP965243.RAkVYL-xnZtV7-xeykch6ZJjBGx8Ubf4XwT6KQXkfUHME130_assertion description "[Infantile neuronal ceroid lipofuscinosis (INCL; NCL1, Haltia-Santavuori disease) is caused by mutations in the CLN1/PPT gene which are associated with an early onset INCL phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP965243.RAkVYL-xnZtV7-xeykch6ZJjBGx8Ubf4XwT6KQXkfUHME130_provenance.