Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_assertion> ?p ?o ?g. }
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- NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_assertion type Assertion NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_head.
- NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_assertion description "[Loss of CSTB function due to mutations is consistent with the observed neurodegenerative pathology and phenotype, but the functional link to the epileptic phenotype of EPM1 remains largely unknown.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_provenance.
- NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_assertion evidence source_evidence_literature NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_provenance.
- NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_assertion SIO_000772 14526183 NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_provenance.
- NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_assertion wasDerivedFrom befree-20150227 NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_provenance.
- NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_assertion wasGeneratedBy ECO_0000203 NP333846.RAd4FX0Igm6oly7QZYuPiTsl_Wh2DqEh-tCotfYyHsV5s130_provenance.