Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP848368.RA9roRW-fq14wyyBR70yVWSQwbCWt6tgDiNmocTuMpxoQ#assertion> ?p ?o ?g. }
Showing items 1 to 5 of
5
with 100 items per page.
- assertion wasGeneratedBy ECO_0000203 provenance.
- assertion wasDerivedFrom BEFREE provenance.
- assertion SIO_000772 22387303 provenance.
- assertion evidence source_evidence_literature provenance.
- 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." provenance.