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- source_evidence_literature type ECO_0000212 NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_provenance.
- NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_assertion description "[Severe Meesmann's epithelial corneal dystrophy phenotype due to a missense mutation in the helix-initiation motif of keratin 12.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_provenance.
- NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_assertion evidence source_evidence_literature NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_provenance.
- NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_assertion SIO_000772 23222558 NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_provenance.
- NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_assertion wasDerivedFrom befree-20150227 NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_provenance.
- NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_assertion wasGeneratedBy ECO_0000203 NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_provenance.
- befree-20150227 importedOn "2015-02-27" NP529033.RARaof26l8ttuaw6YkxYyDxTzjh-8PEhj8kM9iTeWSO50130_provenance.