Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_assertion type Assertion NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_head.
- NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_assertion description "[Tripeptidyl peptidase 1 (TPP1) deficiency causes CLN2 disease, late infantile (or classic late infantile neuronal ceroid lipofuscinosis), a paediatric neurodegenerative disease of autosomal recessive inheritance.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_provenance.
- NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_assertion evidence source_evidence_literature NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_provenance.
- NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_assertion SIO_000772 23587805 NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_provenance.
- NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_assertion wasDerivedFrom befree-20140225 NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_provenance.
- NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_assertion wasGeneratedBy ECO_0000203 NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_provenance.