Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_provenance.
- NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_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." NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_provenance.
- NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_assertion evidence source_evidence_literature NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_provenance.
- NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_assertion SIO_000772 2504515 NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_provenance.
- NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_assertion wasDerivedFrom befree-2016 NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_provenance.
- NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_assertion wasGeneratedBy ECO_0000203 NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_provenance.
- befree-2016 importedOn "2016-02-19" NP1203502.RA_QmbYEkt0jdLqpVy3ETndcGBOOgbQHz5joMuQ4lVyMA130_provenance.