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- source_evidence_literature type ECO_0000212 NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_provenance.
- NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_assertion description "[Mutations in the CDKL5 gene (also known as STK9) have recently been shown to cause early onset epilepsy and severe mental retardation (ISSX or West syndrome).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_provenance.
- NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_assertion evidence source_evidence_literature NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_provenance.
- NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_assertion SIO_000772 16015284 NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_provenance.
- NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_assertion wasDerivedFrom befree-20150227 NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_provenance.
- NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_assertion wasGeneratedBy ECO_0000203 NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978119.RAT7UznhCr9WOY6ENANHOP-4j_Pywuk5QQHNtGEtjlWeo130_provenance.