Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_provenance.
- NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_assertion description "[Further study of the pathological mechanisms of the mutant forms of seipin may lead to important new insights into motor neuron diseases, including other spastic paraplegia diseases and amyotrophic lateral sclerosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_provenance.
- NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_assertion evidence source_evidence_literature NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_provenance.
- NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_assertion SIO_000772 18790819 NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_provenance.
- NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_assertion wasDerivedFrom befree-20150227 NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_provenance.
- NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_assertion wasGeneratedBy ECO_0000203 NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP883898.RA17aysI3FyhxEnZS9NjgUs_MIFNYcCPV0wO0V2PYo2JQ130_provenance.