Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_provenance.
- NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_assertion description "[Murine succinate semialdehyde dehydrogenase (SSADH) deficiency (OMIM 271980; EC 1.2.1.24), a model of the corresponding human disorder, displays 100% mortality at weeks 3-4 of life, associated with lethal tonic-clonic seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_provenance.
- NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_assertion evidence source_evidence_literature NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_provenance.
- NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_assertion SIO_000772 15093183 NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_provenance.
- NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_assertion wasDerivedFrom befree-20150227 NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_provenance.
- NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_assertion wasGeneratedBy ECO_0000203 NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP785963.RA5bkiDZSon31YvhpFyTKMi09xRbxEg7KnfrvaiF0kBIQ130_provenance.