Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_provenance.
- NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_assertion description "[Mutations in tripeptidyl-peptidase I (TPP I) underlie the classic late-infantile form of neuronal ceroid lipofuscinoses (CLN2), the most common neurodegenerative disorders of childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_provenance.
- NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_assertion evidence source_evidence_literature NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_provenance.
- NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_assertion SIO_000772 16895480 NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_provenance.
- NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_assertion wasDerivedFrom befree-20140225 NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_provenance.
- NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_assertion wasGeneratedBy ECO_0000203 NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP180332.RAZGMfRUhmG4WUSdVRMpY9fnDQnAQKxYxRe8B8gFfKIPs130_provenance.