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- source_evidence_literature type ECO_0000212 NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_provenance.
- NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_assertion description "[Mutations in the human CDKL5 gene have been shown to cause infantile spasms, as well as Rett syndrome-like phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_provenance.
- NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_assertion evidence source_evidence_literature NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_provenance.
- NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_assertion SIO_000772 21107515 NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_provenance.
- NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_assertion wasDerivedFrom befree-2016 NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_provenance.
- NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_assertion wasGeneratedBy ECO_0000203 NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_provenance.
- befree-2016 importedOn "2016-02-19" NP854748.RANjvayts2cwjahh_BTEwNGN8W_1oqJYXc_UNe8g9Ajkc130_provenance.