Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_provenance.
- NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_assertion description "[The epilepsy that occurs in SSADH deficiency has a seizure phenotype similar to that occurring in the SSADH(-/-) mouse.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_provenance.
- NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_assertion evidence source_evidence_literature NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_provenance.
- NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_assertion SIO_000772 16240371 NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_provenance.
- NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_assertion wasDerivedFrom befree-2016 NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_provenance.
- NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_assertion wasGeneratedBy ECO_0000203 NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_provenance.
- befree-2016 importedOn "2016-02-19" NP518986.RA1F0yFS8RbwN3v2D9AVDei1n7PTqzcQP5laTad9Rg2ns130_provenance.