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- source_evidence_literature type ECO_0000212 NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_provenance.
- NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_assertion description "[Together with previous reports, our study further indicates that genetic testing of SCN8A should be considered in children with unclassified severe epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_provenance.
- NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_assertion evidence source_evidence_literature NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_provenance.
- NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_assertion SIO_000772 24888894 NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_provenance.
- NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_assertion wasDerivedFrom befree-2016 NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_provenance.
- NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_assertion wasGeneratedBy ECO_0000203 NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP1188067.RAdsekaOc2uHHRyiBG9lIU4i02B_0UAwYXXs0wg4OpelQ130_provenance.