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- source_evidence_literature type ECO_0000212 NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_provenance.
- NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_assertion description "[Fatal familial insomnia (FFI) is an autosomal dominant prion disease clinically characterized by inattention, sleep loss, dysautonomia, and motor signs and pathologically characterized by a preferential thalamic degeneration.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_provenance.
- NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_assertion evidence source_evidence_literature NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_provenance.
- NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_assertion SIO_000772 10389103 NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_provenance.
- NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_assertion wasDerivedFrom befree-20150227 NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_provenance.
- NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_assertion wasGeneratedBy ECO_0000203 NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP647641.RAEvlD-vv7_NzoD1ac_f4o6pyMRaDhExFNCfniNiARSEQ130_provenance.