Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_provenance.
- NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_assertion description "[Autosomal recessive mutations in the ALS2 gene have been linked to juvenile-onset amyotrophic lateral sclerosis (ALS2), primary lateral sclerosis and juvenile-onset ascending hereditary spastic paraplegia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_provenance.
- NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_assertion evidence source_evidence_literature NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_provenance.
- NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_assertion SIO_000772 18714162 NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_provenance.
- NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_assertion wasDerivedFrom befree-20140225 NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_provenance.
- NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_assertion wasGeneratedBy ECO_0000203 NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP487470.RAwrc13GiX0T_fzDP9CdlCYny3FZ2Jv-Ai0kLZfzjeWJM130_provenance.