Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_provenance.
- NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_assertion description "[CSTB homozygous knockout mice show some parallels to the phenotype of human EPM1 including myoclonic seizures, development of ataxia and neuropathological changes associated with cell loss via apoptosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_provenance.
- NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_assertion evidence source_evidence_literature NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_provenance.
- NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_assertion SIO_000772 14526183 NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_provenance.
- NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_assertion wasDerivedFrom befree-20150227 NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_provenance.
- NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_assertion wasGeneratedBy ECO_0000203 NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_provenance.
- befree-20150227 importedOn "2015-02-27" NP333857.RA_qMzbkRWTVw5R5JbWI9Tj8ZPT6lpdkiEZzwSS2jqlcA130_provenance.