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- source_evidence_literature type ECO_0000212 NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_provenance.
- NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_assertion description "[Twenty-eight patients with early onset SMEI/DS before 6 months negative for SCN1A mutational screening were selected and screened for mutations in the ARX gene in males (n=14) or the CDKL5 gene in females (n=14).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_provenance.
- NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_assertion evidence source_evidence_literature NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_provenance.
- NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_assertion SIO_000772 19734009 NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_provenance.
- NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_assertion wasDerivedFrom befree-2016 NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_provenance.
- NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_assertion wasGeneratedBy ECO_0000203 NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_provenance.
- befree-2016 importedOn "2016-02-19" NP761543.RAuhpBTch9HoYnEzydttVprN4nsSt94eG9GNBcw7kOE-E130_provenance.