Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_provenance.
- NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_assertion description "[Severe deficiency of acid ceramidase activity (4-5% of normal) was demonstrated in cultured skin fibroblasts, leukocytes and plasma from a 1-year-old boy who was diagnosed as being affected with Farber disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_provenance.
- NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_assertion evidence source_evidence_literature NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_provenance.
- NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_assertion SIO_000772 2504515 NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_provenance.
- NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_assertion wasDerivedFrom befree-20140225 NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_provenance.
- NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_assertion wasGeneratedBy ECO_0000203 NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_provenance.
- befree-20140225 importedOn "2014-02-25" NP681104.RACXeO0WPGXAjBJdQV-1ZkxdtMNiMrgr8QNPvYm2bazig130_provenance.