Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP765271.RAWxsPJWt0qUma6EPfgDIM_4qkmXQNmvmHudjLmwWMumU130_provenance.