Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_provenance.
- NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_assertion description "[Genetic analysis of PRRT2 for benign infantile epilepsy, infantile convulsions with choreoathetosis syndrome, and benign convulsions with mild gastroenteritis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_provenance.
- NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_assertion evidence source_evidence_literature NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_provenance.
- NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_assertion SIO_000772 23073245 NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_provenance.
- NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_assertion wasDerivedFrom befree-20150227 NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_provenance.
- NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_assertion wasGeneratedBy ECO_0000203 NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_provenance.
- befree-20150227 importedOn "2015-02-27" NP963551.RAVDH62WgUFfO9By2y_KrPKRPzXwVwAEVPqSxhk24HT-Q130_provenance.