Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_provenance.
- NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_assertion description "[Catalytic deficiency of human aldolase B in hereditary fructose intolerance caused by a common missense mutation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_provenance.
- NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_assertion evidence source_evidence_curated NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_provenance.
- NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_assertion SIO_000772 3383242 NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_provenance.
- NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_assertion wasDerivedFrom ctd_human-20150221 NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_provenance.
- NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_assertion wasGeneratedBy ECO_0000218 NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_provenance.
- ctd_human-20150221 importedOn "2015-02-21" NP6689.RALvCpexguxeLySf85X5YXon5JcEyIW0_fub3yTM-9kU8130_provenance.