Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_provenance.
- NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_assertion description "[EKV3 is also characterized by ichthyosis, sensorineural hearing loss, peripheral neuropathy, psychomotor retardation, congenital chronic diarrhea, and an elevation of very long chain fatty acids (VLCFAs).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_provenance.
- NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_assertion evidence source_evidence_literature NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_provenance.
- NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_assertion SIO_000772 15668823 NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_provenance.
- NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_assertion wasDerivedFrom befree-2016 NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_provenance.
- NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_assertion wasGeneratedBy ECO_0000203 NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_provenance.
- befree-2016 importedOn "2016-02-19" NP477816.RAt3yAnQhYUOp43JscytariTpsseUbPgvFdCyRAF3NLlM130_provenance.