Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_assertion type Assertion NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_head.
- NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_assertion description "[We report on a patient who had carried a clinical diagnosis of PDE for 7 years, but who was than shown to have normal ALDH7A1 sequencing and the absence of biomarkers characteristic of this familial epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_provenance.
- NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_assertion evidence source_evidence_literature NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_provenance.
- NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_assertion SIO_000772 23166088 NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_provenance.
- NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_assertion wasDerivedFrom befree-20150227 NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_provenance.
- NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_assertion wasGeneratedBy ECO_0000203 NP256728.RANLV0XC-S40reFQb0HCpbAhzxCPRSW0z_njSOhWOx8rw130_provenance.