Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_provenance.
- befree-2016 importedOn "2016-02-19" NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_provenance.
- NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_assertion wasGeneratedBy ECO_0000203 NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_provenance.
- NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_assertion wasDerivedFrom befree-2016 NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_provenance.
- NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_assertion SIO_000772 10428067 NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_provenance.
- NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_assertion evidence source_evidence_literature NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_provenance.
- NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_assertion description "[A survey of fibroblasts and lymphoblasts demonstrated that lack of activity was associated with LINCL arising from mutations in the CLN2 gene but not other neuronal ceroid lipofuscinoses (NCLs), including the CLN6 variant LINCL, classical infantile NCL, classical juvenile NCL, and adult NCL (Kufs' disease).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP258975.RA4bxUfXQmfQ71M_2_pNQ4NoWJWePM6WHRVSXHHumkd1E130_provenance.