Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_assertion type Assertion NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_head.
- NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_assertion description "[De novo mutations in HCN1 cause early infantile epileptic encephalopathy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_provenance.
- NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_assertion evidence source_evidence_curated NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_provenance.
- NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_assertion SIO_000772 24747641 NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_provenance.
- NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_assertion wasDerivedFrom ctd_human-2016 NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_provenance.
- NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_assertion wasGeneratedBy ECO_0000218 NP33988.RADQsT0UrGlqhQr-R_RisNu6SUfw18kDRKCDMpyUkqoJE130_provenance.