Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_provenance.
- NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_assertion description "[The neuronal ceroid lipofuscinoses (NCL; Batten disease) are a collection of autosomal recessive disorders characterized by the accumulation of autofluorescent lipopigments in the neurons and other cell types.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_provenance.
- NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_assertion evidence source_evidence_literature NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_provenance.
- NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_assertion SIO_000772 8279474 NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_provenance.
- NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_assertion wasDerivedFrom befree-20140225 NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_provenance.
- NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_assertion wasGeneratedBy ECO_0000203 NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP395359.RAwNvhgO870qW-99RVx9FHJZ0STTgiW6J0HziwVEQU8p0130_provenance.