Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_provenance.
- NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_assertion wasGeneratedBy ECO_0000203 NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_provenance.
- NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_assertion wasDerivedFrom befree-20150227 NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_provenance.
- NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_assertion SIO_000772 10428067 NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_provenance.
- NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_assertion evidence source_evidence_literature NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_provenance.
- NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_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." NP585710.RAXFANACrIe-aQG-BvveKeOXlaZSiOEQ8YkS8lP3zDTiQ130_provenance.